A listing of diseases. A disease is an abnormal condition of the body or mind that causes discomfort, dysfunction, or distress to the person afflicted or those in contact with the person. ...

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z A listing of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ... A list of diseases in the English wikipedia. ...

Aa-Ab

• Aagenaes syndrome
• Aarskog Ose Pande syndrome
• Aarskog syndrome
• Aase Smith syndrome
• Aase syndrome
• ABCD syndrome
• Abdallat Davis Farrage syndrome
• Abdominal aortic aneurysm
• Abdominal cystic lymphangioma
• Abdominal defects
• Abdominal musculature absent microphthalmia joint laxity
• Abdominal neoplasms
• Aberrant subclavian artery
• Ablepharon macrostomia syndrome
• Ablutophobia
• Abnormal systemic venous return
• Abruzzo Erickson syndrome
• Absence of Gluteal muscle
• Absence of tibia with polydactyly
• Absent corpus callosum cataract immunodeficiency
• Absent T lymphocytes

Aagenaes syndrome is due to congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant-cell hepatitis with fibrosis of the portal tracts. ... SHORT syndrome is a medical condition in which affected individuals have multiple birth defects in different organ systems. ... Aarskog syndrome is an inherited disease characterized by short stature, facial abnormalities, musculoskeletal, and genital anomalies. ... Aase syndrome or Aase-Smith syndrome is a rare inherited disorder characterized by anemia with some joint and skeletal deformities. ... Aase syndrome or Aase-Smith syndrome is a rare inherited disorder characterized by anemia with some joint and skeletal deformities. ... ABCD syndrome is the acronym for albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness. ... Abdallat Davis Farrage syndrome is a syndrome consisting of disordered skin and hair pigmentation, progressive spastic paraparesis and peripheral neuropathy. ... This article is in need of attention. ... Lymphangioma is a benign proliferation of tumored lymph vessels, and are rare. ... An infant born with an abdominal wall defect has an abnormal opening on the abdomen. ... Normal anatomical locations of right and left subclavian arteries Aberrant subclavian artery, or aberrant subclavian artery syndrome refers to a rare anatomical variant of the origin of the right or left subclavian artery. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... Some characteristics of Abruzzo Erickson syndrome include deafness, protruding ears, a cleft palate, and short stature. ... In 1976 a brother and sister were described with congenital absence of gluteal muscles and with spina bifida occulta. ...

Ac

Aca-Acc

• Acalvaria
• Acanthocheilonemiasis
• Acanthocytosis chorea
• Acanthocytosis
• Acanthosis nigricans muscle cramps acral enlargement
• Acarophobia
• Acatalasemia
• Accessory deep peroneal nerve
• Accessory Navicular bone
• Accessory pancreas

Acalvaria is a rare malformation consisting of absence of the calvarial bones, dura mater and associated muscles in the presence of a normal skull base and normal facial bones. ... Acanthocheilonemiasis is a rare tropical infectious disease caused by a parasite known as Acanthocheilonema perstans. ... Acanthocytes are red blood cells that show many spicules (small needlelike structures) when viewed on a wet film. ... Acatalasemia is a genetic deficiency of erythrocyte catalase. ... Accessory pancreas is a rare condition in which small groups of pancreatic cells are separate from the pancreas. ...

Ach-Ack

• Achalasia alacrimia syndrome
• Achalasia microcephaly
• Achalasia, familial esophageal
• Achalasia
• Achalasia-Addisonianism-Alacrimia syndrome
• Achard syndrome
• Achard-Thiers syndrome
• Acheiropodia
• Achondrogenesis Kozlowski type
• Achondrogenesis type 1A
• Achondrogenesis type 1B
• Achondrogenesis
• Achondroplasia Swiss type agammaglobulinemia
• Achondroplasia
• Achondroplastic dwarfism
• Achromatopsia incomplete, X-linked
• Achromatopsia
• Acid maltase deficiency
• Acidemia, isovaleric
• Acidemia, propionic
• Acitretine antenatal infection
• Ackerman syndrome

Achalasia or acalasia is a failure of a ring of muscle (as a sphincter) to relax (completely). ... Achard syndrome is a syndrome consisting of arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet. ... Achard-Thiers syndrome combines the features of Adrenogenital syndrome and Cushing syndrome. ... Acheiropodia is a congenital defect which consists of bilateral congenital amputations of the upper and lower extremities, as well as aplasia of the hands and feet. ... Achondrogenesis is the most severe form of congenital chondrodysplasia (malformation of bones and cartilage). ... Achondrogenesis is the most severe form of congenital chondrodysplasia (malformation of bones and cartilage). ... Achondrogenesis is a lethal bone disease in utero or a few days after the birth. ... Achondroplasia is a type of genetic disorder that is a common cause of dwarfism. ... Achondroplasia is a type of genetic disorder that is a common cause of dwarfism. ... Achromatopsia is a medical condition (also called maskun or rod monochromatism) characterized by a low cone cell count or lack of function in cone cells; these are the light receptors responsible for color perception. ... Glycogen storage disease type II (also called Pompe disease or acid maltase deficiency) is a rare genetic disorder caused by a deficiency in the enzyme acid alpha-glucosidase (GAA), which is needed to break down glycogen, a stored form of sugar used for energy. ... Isovaleric acidemia is a rare genetic disorder in which the body is unable to process certain proteins properly. ... Propionic acidemia is an inherited disorder of inborn error of intermediary metabolism that may present in the early neonatal period with progressive encephalopathy and death due to a secondary hyperammonemia. ... Ackerman syndrome is a familial syndrome of fused molar roots with a single canal (taurodontism), hypotrichosis, full upper lip without a cupid’s bow, thickened and wide philtrum, and occasional juvenile glaucoma. ...

Acn-Acq

• Acne rosacea
• Acne
• Acoustic neuroma
• Acoustic schwannomas
• Acquired agranulocytosis
• Acquired hypoprothrombinemia
• Acquired Immune Deficiency Syndrome
• Acquired ichthyosis
• Acquired prothrombin deficiency
• Acquired syphilis

Erythematotelangiectatic rosacea, the mildest form of the condition, is characterized by persistent facial redness. ... Acoustic neuroma (or Vestibular Schwannoma) is a benign tumor of the myelin forming cells called Schwann cells of the 8th cranial nerve, known as the acoustic nerve, (or more properly the vestibulocochlear nerve) just after it has left the brainstem, in the pontine angle; also at the point where the... Acoustic neuroma (or Vestibular Schwannoma) is a benign tumor of the myelin forming cells called Schwann cells of the 8th cranial nerve, known as the acoustic nerve, (or more properly the vestibulocochlear nerve) just after it has left the brainstem, in the pontine angle; also at the point where the... The Red Ribbon is a symbol for solidarity with HIV-positive people and those living with AIDS. Acquired immunodeficiency syndrome or acquired immune deficiency syndrome (AIDS or Aids) is a collection of symptoms and infections in humans resulting from the specific damage to the immune system caused by infection with... Ichthyosis acquisita (or acquired ichthyosis) is a disorder clinically and histologically similar to ichthyosis vulgaris. ... Depression_era U.S. poster advocating early syphilis treatment Syphilis (historically called lues) is a sexually transmitted disease (STD) that is caused by a spirochaete bacterium, Treponema pallidum. ...

Acr

Acra

• Acral dysostosis dyserythropoiesis
• Acral renal mandibular syndrome

Acro

• Acro coxo mesomelic dysplasia
• Acro fronto facio nasal dysostosis

Acroc-Acrok

• Acrocallosal syndrome, Schinzel type
• Acrocephalopolydactyly
• Acrocephalosyndactyly Jackson Weiss type
• Acrocephaly pulmonary stenosis mental retardation
• Acrodermatitis enteropathica
• Acrodermatitis
• Acrodysostosis
• Acrodysplasia scoliosis
• Acrofacial dysostosis ambiguous genitalia
• Acrofacial dysostosis atypical postaxial
• Acrofacial dysostosis Catania form
• Acrofacial dysostosis Preis type
• Acrofacial dysostosis Rodriguez type
• Acrofacial dysostosis Weyers type
• Acrofacial dysostosis, Nager type
• Acrofacial dysostosis, Palagonia type
• Acrokeratoelastoidosis of Costa

Acrodermatitis enteropathica is an autosomal recessive disorder characterized by periorificial (around the natural orifices) and acral (in the limbs) dermatitis, alopecia (loss of hair), and diarrhea. ... The term Acrofacial Dysostosis was coined in 1948 by Nager and DeReynier. ...

Acrom-Acros

• Acromegaloid changes cutis verticis gyrata corneal
• Acromegaloid facial appearance syndrome
• Acromegaloid hypertrichosis syndrome
• Acromegaly
• Acromesomelic dysplasia Brahimi Bacha type
• Acromesomelic dysplasia Campailla Martinelli type
• Acromesomelic dysplasia Hunter Thompson type
• Acromesomelic dysplasia, Maroteaux type
• Acromesomelic dysplasia
• Acromicric dysplasia
• Acroosteolysis dominant type
• Acroosteolysis neurogenic
• Acroosteolysis osteoporosis skull and mandible changes
• Acropectoral syndrome
• Acropectorenal field defect
• Acropectorovertebral dysplasia
• Acrophobia
• Acropigmentation of Dohi
• Acrorenal syndrome recessive
• Acrorenoocular syndrome
• Acrospiroma

Rondo Hatton, a famous sufferer of acromegaly whose face was distorted by the disorder. ... Acrophobia (from Greek ἄκρος, meaning summit) is an extreme or irrational fear of heights. ... An acrospiroma is a tumor of the distal portion of a sweat gland. ...

Act

• ACTH deficiency
• ACTH resistance
• Atelectasis
• Actinomycetales infection
• Actinomycosis
• Activated protein C resistance

Adrenocorticotropic hormone deficiency (ACTH deficiency) is a result of a decreased or absent production of adrenocorticotropic hormone (ACTH) by the pituitary gland. ... Glucocorticoid deficiency 1 is an adrenocortical failure characterized by low levels of plasma cortisol despite high levels of plasma ACTH. External links OMIM 202200 Category: ... Atelectasis is defined as collapse of a part of the lung or the whole lung, where the alveoli are deflated, as distinct from pulmonary consolidation. ... Suborders Actinomycineae Corynebacterineae Frankineae Glycomycineae Micrococcineae Micromonosporineae Propionibacterineae Pseudonocardineae Streptomycineae Streptosporangineae Actinomycetales is an order of bacteria belonging to the Actinobacteria. ... Activated protein C resistance is a hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). ...

Acu

Acut

Acuta

• Acutane embryopathy

Isotretinoin is a generic medication used for the treatment of severe acne and most commonly known under the brands Accutane, Roaccutane, Amnesteem, Isotane and Sotret. ...

Acute

Acute a-Acute l

• Acute articular rheumatism
• Acute erythroblastic leukemia
• Acute febrile neutrophilic dermatosis
• Acute idiopathic polyneuritis
• Acute intermittent porphyria
• Acute lymphoblastic leukemia congenital sporadic aniridia
• Acute lymphoblastic leukemia
• Acute lymphocytic leukemia

Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute febrile neutrophilic dermatosis (also known as Sweets syndrome) is a dermatological condition characterized by large, rapidly extending, erythematous, tender plaques on the upper body. ... The porphyrias are inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). ... Acute lymphoblastic leukaemia (ALL), also known as acute lymphocytic leukaemia, is a cancer of the white blood cells, characterised by the overproduction and continuous multiplication of malignant and immature white blood cells (referred to as lymphoblasts) in the bone marrow. ... Acute lymphocytic leukaemia (ALL), also known as acute lymphoblastic leukaemia is a cancer of the white blood cells, characterised by the overproduction and continuous multiplication of malignant and immature white blood cells (referred to as lymphoblasts) in the bone marrow. ...

Acute m-Acute r

• Acute megakaryoblastic leukemia
• Acute monoblastic leukemia
• Acute mountain sickness
• Acute myeloblastic leukemia type 1
• Acute myeloblastic leukemia type 2
• Acute myeloblastic leukemia type 3
• Acute myeloblastic leukemia type 4
• Acute myeloblastic leukemia type 5
• Acute myeloblastic leukemia type 6
• Acute myeloblastic leukemia type 7
• Acute myeloblastic leukemia with maturation
• Acute myeloblastic leukemia without maturation
• Acute myelocytic leukemia
• Acute myelogenous leukemia
• Acute myeloid leukemia (generic term)
• Acute myeloid leukemia, secondary
• Acute myelomonocytic leukemia
• Acute necrotizing ulcerative gingivitis
• Acute non lymphoblastic leukemia (generic term)
• Acute posterior multifocal placoid pigment epitheliopathy
• Acute promyelocytic leukemia
• Acute renal failure
• Acute respiratory distress syndrome
• Acute tubular necrosis

Altitude sickness, also known as acute mountain sickness (AMS) or altitude illness is a pathological condition that is caused by lack of adaptation to high altitudes. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of white blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Trench mouth is a polymicrobial infection of the gums leading to inflammation, bleeding, deep ulceration and necrotic gum tissue, there may also be fever. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. ... Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of white blood cells. ... Acute respiratory distress syndrome (ARDS), also known as respiratory distress syndrome (RDS) or adult respiratory distress syndrome (in contrast with IRDS) is a serious reaction to various forms of injuries to the lung. ... Acute tubular necrosis may be toxic or ischemic. ...

Acy

• Acyl-CoA dehydrogenase, medium chain, deficiency of
• Acyl-CoA dehydrogenase, short chain, deficiency of
• Acyl-CoA dehydrogenase, very long chain, deficiency of
• Acyl-CoA oxidase deficiency

Medium-chain acyl-coenzyme A dehydrogenase deficiency is one of a group of conditions that is associated with inborn errors of metabolism in fatty acid oxidation. ... Short-chain acyl-coenzyme A dehydrogenase deficiency (or SCAD) is a fatty acid metabolism disorder. ... Very long-chain acyl-coenzyme A dehydrogenase deficiency is a condition that prevents the body from converting certain fats to energy, particularly during periods without food. ...

Ad

Ada-Adi

• Adactylia unilateral dominant
• Adam complex familial
• Adams Nance syndrome
• Adams-Oliver syndrome
• Addison's disease
• Adducted thumb club foot syndrome
• Adducted thumb syndrome recessive form
• Adducted thumbs Dundar type
• Adenine phosphoribosyltransferase deficiency
• Adenocarcinoid tumor
• Adenocarcinoma of lung
• Adenoid cystic carcinoma
• Adenoma of the adrenal gland
• Adenoma
• Adenomelablastoma
• Adenomyosis
• Adenosine deaminase deficiency
• Adenosine monophosphate deaminase deficiency
• Adenosine triphosphatase deficiency, anemia due to
• Adenylosuccinate lyase deficiency
• Adie syndrome
• Adiposis dolorosa aka Dercum's disease

Adams Nance syndrome is a syndrome consisting of persistent tachycardia, paroxymal hypertension and seizures. ... Adams-Oliver syndrome is a rare syndrome of defects of the scalp and cranium associated with distal limb anomalies and occasional mental retardation. ... Addisons disease (also known as chronic adrenal insufficiency, or hypocortisolism) is a rare endocrine disorder. ... Adducted thumb syndrome recessive form is a rare disease also known as Christian syndrome or Craniosynostosis arthrogryposis cleft palate. ... 2,8 dihydroxy-adenine urolithiasis (also called adenine phosphoribosyltransferase deficiency) is an autosomal recessive disorder resulting in accumulation and urinary excretion of the insoluble purine 2,8-dihydroxyadenine. ... Lung cancer is a cancer of the lungs characterised by the presence of malignant tumours. ... Adenoid cystic cancer (AdCC) is a very rare type of cancer that can exist in many different body sites. ... It has been suggested that this article or section be merged into Adenoma#Adrenal_. ... Adenoma refers to a collection of growths (-oma) of glandular origin. ... Adenomyosis is a medical condition characterized by the presence of ectopic endometrial tissue (the inner lining of the uterus) within the myometrium (the thick, muscular layer of the uterus). ... Adenosine deaminase deficiency, or ADA deficiency, is an inherited immunodeficiency syndrome accounting for about 25% of all cases of Severe combined immunodeficiency. ... Myoadenylate deaminase deficiency (MADD) is a recessive genetic metabolic disorder that affects approximately 1-2% of populations of European descent (making it a not particularly rare rare disease). ... Adenylosuccinate lyase deficiency is a heritable deficiency which is characterized by the appearance of succinylaminoimidazolecarboxamide riboside (SAICAriboside) and succinyladenosine (S-Ado) in cerebrospinal fluid, urine, and to a lesser extent in plasma [1]. These two succinylpurines are the dephosphorylated derivatives of SAICAribotide (SAICAR) and adenylosuccinate (S-AMP), the two substrates... Adie syndrome is caused by damage to the postganglionic fibers of the parasympathetic innervation of the eye and characterized by a tonically dilated pupil. ... Adiposis dolorosa is a rare disease characterized by multiple painful lipomas that arise in adult life. ...

Ado-Adr

• Adolescent benign focal crisis
• Adrenal adenoma, familial
• Adrenal cancer
• Adrenal disorder
• Adrenal gland hyperfunction
• Adrenal gland hypofunction
• Adrenal hyperplasia, congenital
• Adrenal hyperplasia
• Adrenal hypertension
• Adrenal hypoplasia congenital, X-linked
• Adrenal hypoplasia
• Adrenal incidentaloma
• Adrenal insufficiency
• Adrenal macropolyadenomatosis
• Adrenal medulla neoplasm
• Adrenocortical carcinoma
• Adrenogenital syndrome
• Adrenoleukodystrophy, autosomal, neonatal form
• Adrenoleukodystrophy, X-linked
• Adrenoleukodystrophy
• Adrenomyodystrophy

Adrenal tumor in pink Adrenal cancer is a rare disease that afflicts the adrenal gland. ... Congenital adrenal hyperplasia (CAH) refers to any of several autosomal recessive diseases resulting from defects in steps of the synthesis of cortisol from cholesterol by the adrenal glands. ... Congenital adrenal hyperplasia (CAH) refers to any of several autosomal recessive diseases resulting from defects in steps of the synthesis of cortisol from cholesterol by the adrenal glands. ... In medicine, an incidentaloma is a tumor (_oma) found by coincidence (incidental) without clinical symptoms and suspicion. ... In medicine, adrenal insufficiency (or hypocortisolism) is the inability of the adrenal gland to produce adequate amounts of cortisol in response to stress. ... Adrenocortical carcinoma is a carcinoma of the cortex (outer layer) of the adrenal gland. ... Congenital adrenal hyperplasia (CAH) refers to any of several autosomal recessive diseases resulting from defects in steps of the synthesis of cortisol from cholesterol by the adrenal glands. ... Adrenoleukodystrophy (ALD) is a degenerative disorder of the fatty white sheath covering nerve fibers, known as myelin. ... Adrenoleukodystrophy (ALD) is a degenerative disorder of the fatty white sheath covering nerve fibers, known as myelin. ... Adrenoleukodystrophy (ALD) is a degenerative disorder of the fatty white sheath covering nerve fibers, known as myelin. ...

Adu

• Adult onset Still's disease
• Adult spinal muscular atrophy
• Adult syndrome

Stills disease is a form of juvenile rheumatoid arthritis (JRA), characterized by high spiking fevers and transient rashes, named after the English physician Sir George F. Still (1861-1941). ...

Ae-Ah

• Afibrinogenemia
• Aganglionosis, total intestinal
• Aging
• Aggressive fibromatosis
• Agnathia holoprosencephaly situs inversus
• Agnosia, primary visual
• Agoraphobia
• Agyria pachygyria polymicrogyria
• Agyria-pachygyria type 1
• Ahumada-Del Castillo syndrome

Congenital afibrinogenemia is a rare inherited blood disorder in which the blood does not clot normally due to a lack of or a malfunction involving fibrinogen, a protein necessary for coagulation. ... It has been suggested that this article or section be merged into Ageing. ... Agoraphobia is a form of anxiety disorder. ...

Ai-Ak

• Aicardi syndrome
• Aicardi-Goutieres syndrome
• Aichmophobia
• AIDS Dementia Complex
• AIDS dysmorphic syndrome
• Ainhum
• Akaba Hayasaka syndrome
• Akesson syndrome
• Aksu Stckhausen syndrome

Aicardi syndrome is a congenital disorder thought to result from an abnormality of the X chromosome and characterized by absence of the corpus callosum, retinal abnormalities, and seizures (often infantile spasms). ... Aichmophobia is the fear of knives, needles, or other sharp, pointed objects. ... AIDS dementia complex (ADC) is one of the most common neurological complications of late HIV infection. ... Ainhum disease is the autoamputation of the fifth toe. ...

Al

• Al Awadi Teebi Farag syndrome
• Al Frayh Facharzt Haque syndrome
• Al Gazali Al Talabani syndrome
• Al Gazali Aziz Salem syndrome
• Al Gazali Donnai Mueller syndrome
• Al Gazali Hirschsprung syndrome
• Al Gazali Khidr Prem Chandran syndrome
• Al Gazali Sabrinathan Nair syndrome

Ala-Alc

• Alagille-Watson syndrome (AWS)
• Alar nasal cartilages coloboma of telecanthus
• Albers-Schonberg disease
• Albinism deafness syndrome
• Albinism immunodeficiency
• Albinism ocular late onset sensorineural deafness
• Albinism oculocutaneous, Hermansky-Pudlak type
• Albinism, minimal pigment type
• Albinism, ocular
• Albinism, yellow mutant type
• Albinism
• Albinoidism
• Albrecht Schneider Belmont syndrome
• Albright like syndrome
• Albright Turner Morgani syndrome
• Albright's hereditary osteodystrophy
• Albright's syndrome
• Alcaptonuria
• Alcohol antenatal infection
• Alcohol fetopathy
• Alcoholic hepatitis
• Alcoholic liver cirrhosis

Alagille syndrome is a genetic disorder that affects the liver, heart, and other systems of the body. ... Chédiak-Higashi syndrome is a rare childhood autosomal recessive disorder that affects multiple systems of the body, which arises from a mutation that causes silvery hair. ... Albinism (from Latin albus, meaning white) is a lack of pigmentation in the eyes, skin and hair. ... Albinism (from Latin albus, meaning white) is a lack of pigmentation in the eyes, skin and hair. ... An osteoma (plural: osteomata) is a new piece of bone usually growing on another piece of bone, typically the skull. ... McCune-Albright syndrome, described in 1937 by McCune and Albright, is a disease where two of the three following features are present: (autonomous) endocrine hyperfunction Fibrous dysplasia Café-au-lait spots The endocrine aspect of the disease can manifest itself as extremely premature puberty. ... Alkaptonuria also known as alcaptonuria or ochronosis is a rare inherited genetic disorder of tyrosine metabolism. ... A baby with FAS; his lifetime medical and welfare costs are calculated at $5 million. ... In medicine (gastroenterology), hepatitis is any disease featuring inflammation of the liver. ... Cirrhosis is a chronic disease of the liver in which liver tissue is replaced by connective tissue, resulting in the loss of liver function. ...

Ald-Alk

• Aldolase A deficiency
• Aldred syndrome
• Aleukemic leukemia cutis
• Alexander disease
• Alien hand syndrome
• Alkaptonuria

Alexander disease is a slowly progressing fatal neurodegenerative disease. ... Alien hand syndrome (anarchic hand or Dr. Strangelove syndrome) is an unusual neurological disorder in which one of the sufferers hands seems to take on a life of its own. ... Alkaptonuria also known as alcaptonuria or ochronosis is a rare inherited genetic disorder of tyrosine metabolism. ...

All

• Allain Babin Demarquez syndrome
• Allan Herndon syndrome
• Allanson Pantzar McLeod syndrome
• Allergic angiitis
• Allergic autoimmune thyroiditis
• Allergic bronchopulmonary aspergillosis
• Allergic encephalomyelitis
• Allodoxaphobia

Allergic bronchopulmonary aspergillosis (ABPA) is a hypersensitivity response to the fungus Aspergillus fumigatus, the spores of which are ubiquitous in soil and are commonly found in the sputum of healthy individuals. ...

Alo

• Aloi Tomasini Isaia syndrome
• Alopecia anosmia deafness hypogonadism syndrome
• Alopecia areata
• Alopecia congenita keratosis palmoplantaris
• Alopecia contractures dwarfism mental retardation
• Alopecia epilepsy oligophrenia syndrome of Moynahan
• Alopecia hypogonadism extrapyramidal disorder
• Alopecia immunodeficiency
• Alopecia macular degeneration growth retardation
• Alopecia mental retardation hypogonadism
• Alopecia mental retardation syndrome
• Alopecia totalis
• Alopecia universalis onychodystrophy vitiligo
• Alopecia universalis
• Alopecia, epilepsy, pyorrhea, mental subnormality
• Alopecia

Alopecia totalis is the loss of all head hair. ... John D. Rockefeller, victim of alopecia universalis Alopecia universalis is a medical disorder in which the afflicted are unable to grow hair on the entire body. ... Alopecia is a set of disorders ranging from male and female pattern alopecia (alopecia androgenetica), to alopecia areata, which involves the loss of some of the hair from the head, alopecia totalis, which involves the loss of all head hair, to the most extreme form, alopecia universalis, which involves the...

Alp-Alz

• Alpers disease
• Alpha 1-antitrypsin deficiency
• Alpha-2 deficient collagen disease
• Alpha-ketoglutarate dehydrogenase deficiency
• Alpha-L-iduronidase deficiency
• Alpha-mannosidosis
• Alpha-sarcoglycanopathy
• Alpha-thalassemia
• Alpha-thalassemia-abnormal morphogenesis
• Alport syndrome macrothrombocytopenia
• Alport syndrome, dominant type
• Alport syndrome, recessive type
• Alport syndrome
• Alstrom's syndrome
• Alternating hemiplegia of childhood
• Alternating hemiplegia
• Aluminium lung
• Alveolar echinococcosis
• Alveolar soft part sarcoma
• Alveolitis, extrinsic allergic
• Alves Dos Santos Castello syndrome
• Alzheimer's disease
• Alzheimer disease, familial

Alpers disease, also called progressive infantile poliodystrophy, is a progressive degenerative disease of the central nervous system that occurs in infants and children. ... Alpha 1-antitrypsin deficiency (A1AD or Alpha-1) is a genetic disorder caused by reduced levels of alpha 1-antitrypsin in the blood. ... α-mannosidosis is a genetic disorder that causes progressive mental and physical deterioration. ... Thalassemia (American English) (or thalassaemia in British English) is an inherited disease of the red blood cells, classified as a hemoglobinopathy. ... Alport syndrome is a hereditary disease characterized by hematuria. ... Alternating Hemiplegia is a rare neurological disorder that manifests itself in the paralysis of one side of the body in recurring episodes. ... Hypersensitivity pneumonitis (also called extrinsic allergic alveolitis) is an inflammation of the lung caused by the bodys immune reaction to small air-borne particles. ... Familial Alzheimers disease (FAD) is an uncommon form of Alzheimers disease that comes on earlier in life, defined as before the age of 65 (usually between 30 and 65 years of age) and is inherited in an autosomal dominant fashion. ...

Am

Ama-Ame

• Amathophobia
• Amaurosis
• Amaurosis congenita of Leber, type 1
• Amaurosis congenita of Leber, type 2
• Amaurosis congenita of Leber
• Amaurosis hypertrichosis
• Amaxophobia
• Amblyopia
• Ambral syndrome
• Ambras syndrome
• Ambulophobia
• Amegakaryocytic thrombocytopenia
• Amelia cleft lip palate hydrocephalus iris coloboma
• Amelia facial dysmorphism
• Amelia X linked
• Amelogenesis Imperfecta hypomaturation type
• Amelogenesis imperfecta local hypoplastic form
• Amelogenesis imperfecta nephrocalcinosis
• Amelogenesis imperfecta
• Ameloonychohypohidrotic syndrome
• Amenorrhea
• American trypanosomiasis

Amaurosis (from greek for darkening, dark or obscure) is a weakness or loss of vision, the cause of which was at one time unknown. ... Amblyopia, or lazy eye, is a disorder of the eye. ... Hypertrichosis lanuginosa also called Congenital hypertrichosis lanuginosa, and congenital hypertrichosis universalis, is a genetic condition characterized by hair all over the body. ... Amelogenesis Imperfecta is an inherited condition that presents abnormal formation of the enamel or external layer of teeth. ... Amenorrhoea (BE) or amenorrhea (AmE) is the absence of a menstrual period in a woman of reproductive age. ... ...

Ami-Amy

• Aminoacidopathies
• Aminoaciduria
• Aminopterin antenatal infection
• Aminopterin like syndrome without aminopterin
• Amniotic bands
• Amoebiasis due to Entamoeba histolytica
• Amoebiasis due to free-living amoebae
• Amoebiasis or Amebiasis
• Ampola syndrome
• Amychophobia
• Amylo-1,6-glucosidase deficiency
• Amyloid angiopathy
• Amyloid Neuropathies, Familial
• Amyloid polyneuropathy, transthyretin related
• Amyloidosis of gingiva and conjunctiva mental retardation
• Amyloidosis, Familial
• Amyloidosis
• Amylopectinosis
• Amyoplasia mandibulofacial dysostosis
• Amyoplasia
• Amyotonia congenita
• Amyotrophic lateral sclerosis

Aminoaciduria is the presence of amino acids in the urine. ... Amoebiasis is infection by an protozoan, typically Entamoeba histolytica. ... Amychophobia is a phobia of persistent, abnormal, and unwarranted fear of scratches or being scratched. ... Amyotrophic lateral sclerosis (ALS, sometimes called Lou Gehrigs disease, Maladie de Charcot or motor neurone disease) is a progressive, almost invariably fatal neurological disease. ...

An

Ana-Ane

• Anablephobia
• Anaphylaxis
• Anaplastic thyroid cancer
• Andersen's disease
• Andre syndrome
• Androgen insensitivity syndrome (AIS)
• Anemia sideroblastic spinocerebellar ataxia
• Anemia, Diamond-Blackfan
• Anemia, Hypoplastic, Congenital
• Anemia, Pernicious
• Anemia, Sideroblastic
• Anemia
• Anencephaly spina bifida X linked
• Anencephaly
• Aneurysm of sinus of Valsalva
• Aneurysm, intracranial berry
• Aneurysm

In medicine, anaphylaxis is a severe and rapid systemic allergic reaction. ... Thyroid cancer is cancer of the thyroid gland. ... Androgen insensitivity syndrome (AIS, or Androgen resistance syndrome) is a set of disorders of sexual differentiation that results from mutations of the gene encoding the androgen receptor. ... Diamond-Blackfan anemia (DBA) is a congenital erythroid aplasia that usually presents in infancy. ... Pernicious anemia refers to a type of autoimmune anemia. ... Sideroblastic anemia is caused by the abnormal production of red blood cells as part of myelodysplastic syndrome, which can evolve into hematological malignancies (especially acute myelogenous leukemia). ... This article discusses the medical condition. ... Baby with Anencephaly in Nepal Anencephaly is a cephalic disorder that results from a neural tube defect that occurs when the cephalic (head) end of the neural tube fails to close, usually between the 23rd and 26th day of pregnancy, resulting in the absence of a major portion of the... Aneurysm of the aortic sinus, also known as the sinus of Valsalva. ... // Headline text For the Nirvana song see Aneurysm (song). ...

Ang

• Angel shaped phalangoepiphyseal dysplasia
• Angelman syndrome
• Angiofollicular ganglionic hyperplasia
• Angiofollicular lymph hyperplasia
• Angioimmunoblastic lymphadenopathy with dysproteinemia
• Angiokeratoma mental retardation coarse face
• Angiolipoma
• Angioma hereditary neurocutaneous
• Angiomatosis encephalotrigeminal
• Angiomatosis leptomeningeal capillary - venous
• Angiomatosis systemic cystic Seip syndrome
• Angiomyomatous Hamartoma
• Angioneurotic edema hereditary due to C1 esterase deficiency
• Angiosarcoma of the liver
• Angiosarcoma of the scalp
• Angiostrongyliasis
• Angiotensin renin aldosterone hypertension
• Anguillulosis

Angelman syndrome (AS) is neurological disorder in which severe learning difficulties are associated with a characteristic facial appearance and behavior. ... Strongyloides stercoralis. ...

Ani-Ank

• Aniridia absent patella
• Aniridia ataxia renal agenesis psychomotor retardation
• Aniridia cerebellar ataxia mental deficiency
• Aniridia mental retardation syndrome
• Aniridia ptosis mental retardation obesity familial
• Aniridia renal agenesis psychomotor retardation
• Aniridia type 2
• Aniridia, sporadic
• Aniridia
• Anisakiasis
• Ankle defects short stature
• Ankyloblepharon ectodermal defects cleft lip palate
• Ankyloblepharon filiforme adnatum cleft palate
• Ankyloblepharon filiforme imperforate anus
• Ankyloglossia heterochromia clasped thumbs
• Ankylosing spondylarthritis
• Ankylosing spondylitis
• Ankylosing vertebral hyperostosis with tylosis
• Ankylosis of teeth
• Ankylostomiasis

Aniridia is a rare congenital eye condition leading to the absence of the iris of the eye. ... Species Anisakis pegreffii Anisakis physeteris Anisakis schupakovi Anisakis simplex Anisakis simplex Anisakis typica Anisakis ziphidarum Anisakis is a genus of parasitic nematodes, which have a life cycle involving fish and marine mammals. ... The hookworm is a parasite that lives in the small intestine of its host, which may be a mammal such as a dog, cat, or human. ...

Ann

• Annular constricting bands
• Annular pancreas
• Annuloaortic ectasia

Annular pancreas is a rare condition in which the duodenum is surrounded by a ring of pancreatic tissue continous with the head of the pancreas. ...

Ano

• Anodontia
• Anonychia ectrodactyly
• Anonychia microcephaly
• Anonychia onychodystrophy brachydactyly type B
• Anonychia onychodystrophy
• Anophthalia pulmonary hypoplasia
• Anophthalmia cleft lip palate hypothalamic disorder
• Anophthalmia cleft palate micrognathia
• Anophthalmia esophageal atresia cryptorchidism
• Anophthalmia megalocornea cardiopathy skeletal anomalies
• Anophthalmia microcephaly hypogonadism
• Anophthalmia plus syndrome
• Anophthalmia short stature obesity
• Anophthalmia Waardenburg syndrome
• Anophthalmos with limb anomalies
• Anophthalmos, clinical
• Anorchia
• Anorchidism
• Anorectal anomalies
• Ano-rectal atresia
• Anorexia nervosa
• Anosmia
• Anotia facial palsy cardiac defect
• Anotia

In dentistry, anodontia, also called anodontia vera, is a rare genetic disorder characterized by the congenital absence of all primary or permanent teeth. ... Anorchia, is a medical condition where both testes are absent at birth. ... Anorchia, is a medical condition where both testes are absent at birth. ... To meet Wikipedias quality standards, this article or section may require cleanup. ... Anosmia is the lack of olfaction, or a loss of the sense of smell. ... Anotia ( no ear) describes a rare, congenital deformity, a missing auricle, the external, visible part of the ear. ...

Ans-Ant

• Ansell Bywaters Elderking syndrome
• Anterior horn disease
• Anterior pituitary insufficiency, familial
• Anthophobia
• Anthrax
• Anti-factor VIII autoimmunization
• Antigen-peptide-transporter 2 deficiency
• Anti-HLA hyperimmunization
• Antihypertensive drugs antenatal infection
• Antinolo Nieto Borrego syndrome
• Antiphospholipid syndrome
• Anti-plasmin deficiency, congenital
• Antisocial personality disorder
• Antisynthetase syndrome
• Antithrombin deficiency, congenital
• Antley-Bixler syndrome
• Antlophobia
• Anton's syndrome

The motor neurone diseases (MND) are a group of progressive neurological disorders that destroy motor neurones, the cells that control voluntary muscle activity such as speaking, walking, breathing, and swallowing. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... Antiphospholipid syndrome (or antiphospholipid antibody syndrome) is a disorder of coagulation which causes thrombosis in both arteries and veins, as well as recurrent miscarriage. ... Antisocial personality disorder (APD or ASPD) is a psychiatric diagnosis that interprets antisocial and impulsive behaviours as symptoms of a personality disorder. ... Antithrombin is a small molecule that inactivates several enzymes of the coagulation system. ... Antons syndrome is a form of cortical blindness in which the patient denies the visual impairment. ...

Ao

• Aorta-pulmonary artery fistula
• Aortic aneurysm
• Aortic arch anomaly peculiar facies mental retardation
• Aortic arch interruption
• Aortic arches defect
• Aortic coarctation
• Aortic dissection
• Aortic dissection lentiginosis
• Aortic supravalvular stenosis
• Aortic valve stenosis
• Aortic valves stenosis of the child
• Aortic window

An aortic aneurysm is a general term for any swelling (dilatation or aneurysm) of the aorta, usually representing an underlying weakness in the wall of the aorta at that location. ... Aortic coarctation is narrowing of the aorta in the area where the ductus arteriosus (ligamentum arteriosum after regression) inserts. ... Aortic dissection is a tear in the wall of the aorta (the largest artery of the body). ... Aortic valve stenosis (AS) is a heart condition caused by the incomplete opening of the aortic valve. ...

Ap

Ape-App

• Apert like polydactyly syndrome
• Apert syndrome
• Aphalangia hemivertebrae
• Aphalangia syndactyly microcephaly
• Aphthous stomatitis
• Apiphobia
• Aplasia cutis autosomal recessive
• Aplasia cutis congenita dominant
• Aplasia cutis congenita epibulbar dermoids
• Aplasia cutis congenita intestinal lymphangiectasia
• Aplasia cutis congenita of limbs recessive
• Aplasia cutis congenita recessive
• Aplasia cutis congenita
• Aplasia cutis myopia
• Aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits and nails
• Aplastic anemia
• Apo A-I deficiency
• Apolipoprotein C-II deficiency
• Apparent mineralocorticoid excess
• Appelt-Gerken-Lenz syndrome
• Appendicitis

Apert Syndrome, virtually synonymous with Acrocephalosyndactyly, is a branchial arch syndrome, characterized by a number of clinical features, resulting from a developmental anomaly. ... A mouth ulcer or canker sore is a painful open sore inside the mouth caused by a break in the mucous membrane. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... Aplastic anemia is a condition where the bone marrow does not produce enough, or any, new cells to replenish the blood cells. ... Apparent mineralocorticoid excess is a an autosomal recessive cause of hypertension and hypokalaemia which responds to glucocorticoid treatment. ... Appendicitis, or epityphlitis, is a condition characterised by inflammation of the appendix. ...

Apr-Apu

• Apraxia manual
• Apraxia, Ideomotor
• Apraxia, ocular motor, Cogan type
• Apraxia
• Apudoma

Apraxia is a neurological disorder characterized by loss of the ability to execute or carry out learned (familiar) movements, despite having the desire and the physical ability to perform the movements. ...

Aq

• Aqueductal stenosis, X linked

Ar

Ara-Aro

• Arachindonic acid, absence of
• Arachnodactyly ataxia cataract aminoaciduria mental retardation
• Arachnodactyly mental retardation dysmorphism
• Arachnoid cysts
• Arachnoiditis
• Arakawa'sa syndrome II
• Arbovirosis
• Arc syndrome
• Aredyld syndrome
• AREDYLD
• Arginase deficiency
• Arginemia
• Argininosuccinate synthetase deficiency
• Argininosuccinic aciduria
• Argyria
• Arhinia choanal atresia microphthalmia
• Arnold Stckler Bourne syndrome
• Arnold-Chiari malformation
• Arnold-Chiari syndrome
• Aromatase deficiency
• Aromatic amino acid decarboxylase deficiency

Arachnoid cysts are cerebrospinal fluid-filled sacs that may develop between the surface of the brain and the cranial base or on the arachnoid membrane - one of the 3 membranes that cover the brain and the spinal cord. ... Arachnoiditis describes a pain disorder caused by the inflammation of the arachnoid, one of the membranes that surround and protect the nerves of the spinal cord. ... Arakawas syndrome II is an inborn error of metabolism, a genetic disorder that causes a deficiency of the enzyme tetrahydrofolate-methyltransferase; affected individuals cannot properly metabolize methylcobalamin, a type of Vitamin B12. ... AREDYLD stands for acral renal ectodermal dysplasia lipoatrophic diabetes. ... Arginemia (also called arginase deficiency) is a congenital disorder where arginase deficiency causes a high level of arginine in the blood. ... Arginemia (also called arginase deficiency) is a congenital disorder where arginase deficiency causes a high level of arginine in the blood. ... Citrullinemia is an inherited disorder that causes ammonia and other toxic substances to accumulate in the blood. ... Argininosuccinic aciduria is an inherited disorder that causes ammonia to accumulate in the blood. ... There is also a village named Argyria in Greece (pronunciation: ar-YEE-ree-a) , see Argyria, Greece. ... Arnold-Chiari malformation, sometimes referred to as the Chiari malformation, is an anomaly of the brain in which the cerebellar tonsils are elongated and pushed down through the opening of the base of the skull (see foramen magnum), blocking the flow of cerebrospinal fluid (CSF). ... Arnold-Chiari malformation, sometimes referred to as Chiari malformation or ACM, is a congenital anomaly of the brain in which the cerebellar tonsils are elongated and pushed down through the opening of the base of the skull (see foramen magnum), blocking the flow of cerebrospinal fluid (CSF). ...

Arr

• Arrhinia
• Arrhythmogenic right ventricular dysplasia
• Arroyo Garcia Cimadevilla syndrome
• Arrythmogenic right ventricular dysplasia, familial

Arrhinia is the absence of the nose at birth. ... Arrhythmogenic right ventricular dysplasia (ARVD, also known as arrhythmogenic right ventricular cardiomyopathy or ARVC) is a type of nonischemic cardiomyopathy that involves primarily the right ventricle. ...

Art

Arte

• Arterial calcification of infancy
• Arterial dysplasia
• Arterial tortuosity
• Arteriovenous malformation
• Arteritis

Arteriovenous malformation or AVM is a congenital disorder of the veins and arteries that make up the vascular system . ... Arteritis is inflammation of the walls of arteries, usually as a result of infection or auto-immune response. ...

Arth

• Arthritis short stature deafness
• Arthritis, Juvenile
• Arthritis
• Arthrogryposis due to muscular dystrophy
• Arthrogryposis ectodermal dysplasia other anomalies
• Arthrogryposis epileptic seizures migrational brain disorder
• Arthrogryposis IUGR thoracic dystrophy
• Arthrogryposis like disorder
• Arthrogryposis like hand anomaly sensorineural
• Arthrogryposis multiplex congenita CNS calcification
• Arthrogryposis multiplex congenita distal
• Arthrogryposis multiplex congenita neurogenic type
• Arthrogryposis multiplex congenita pulmonary hypoplasia
• Arthrogryposis multiplex congenita whistling face
• Arthrogryposis multiplex congenita, distal type 1
• Arthrogryposis multiplex congenita, distal type 2
• Arthrogryposis multiplex congenita, distal, x-linked
• Arthrogryposis multiplex congenita
• Arthrogryposis ophthalmoplegia retinopathy
• Arthrogryposis renal dysfunction cholestasis syndrome
• Arthrogryposis spinal muscular atrophy
• Arthrogryposis

Arthritis(from Greek arthro-, joint + -itis, inflammation) is a group of conditions that affect the health of the bone joints in the body. ... Arthrogryposis multiplex congenita, often simply referred to as arthrogryposis (SAMPA pronunciation: ar. ... Arthrogryposis (Arthrogryposis Multiplex Congenita) is a muscle disorder that causes multiple joint contractures at birth. ...

Ary

• Arylsulfatase A deficiency

As

• Asbestosis
• Ascariasis
• Ascher's Syndrome
• Aseptic meningitis
• Asherman's syndrome
• Aspartylglycosaminuria
• Aspergillosis
• Asphyxia neonatorum
• Asthenia
• Asthenia
• Asthenophobia
• Asthma
• Astrocytoma
• Asymmetric septal hypertrophy

Chest X-ray in asbestosis shows plaques above diaphragm Asbestosis is a chronic inflammatory medical condition affecting the parenchymal tissue of the lungs. ... Binomial name Ascaris lumbricoides Linnaeus, 1758 Ascariasis is a debilitating human disease caused by the parasitic roundworm Ascaris lumbricoides. ... Aseptic meningitis is a condition in which the layers lining of the brain, or meninges, become inflamed and a bacterial or viral source cannot be detected. ... Ashermans syndrome , also called uterine synechiae, presents a condition characterized by the presence of scars within the uterine cavity. ... Aspartylglycosaminuria is an inborn error of metabolism caused by deficient activity of the enzyme aspartylglucosaminidase. ... Perinatal asphyxia is the medical condition resulting from deprivation of oxygen (hypoxia) to a newborn infant long enough to cause apparent harm. ... Asthenia is a medical term denoting weakness, lack of energy and strength. ... Asthenia is a medical term denoting weakness, lack of energy and strength. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... Astrocytomas are intracranial tumors derived from astrocytes. ...

At

• Ataxia telangiectasia variant V1
• Ataxia telangiectasia
• Ataxia, Marie's
• Ataxiophobia
• Ataxophobia
• Atelosteogenesis, type II
• Athabaskan brain stem dysgenesis
• Atherosclerosis
• Athetosis
• Athlete's foot
• Atopic Dermatitis
• Atresia of small intestine
• Atrial myxoma, familial
• Atrial septal defect
• Atrioventricular fistula
• Atrioventricular septal defect
• Atrophoderma of Pierini and Pasini
• Atrophy
• ATR-X
• Attention Deficit Hyperactivity Disorder
• Attenuated FAP
• Atychiphobia
• Atypical lipodystrophy

Ataxia-telangiectasia (AT) (Boder-Sedgwick syndrome or Louis-Bar syndrome) is a primary immunodeficiency disorder that occurs in an estimated incidence of 1 in 40,000 to 1 in 300,000 births (Lederman, 2000). ... Atelosteogenesis, type II is a severe disorder of cartilage and bone development. ... Athetosis is a continuous stream of slow, sinuous, writhing movements, typically of the hands and feet. ... Athletes foot or tinea pedis is a fungal infection of the skin, usually between the toes, caused by parasitic fungi. ... Atrial septal defects (ASD) are a group of congenital heart diseases that involve the interatrial septum of the heart. ... An atrioventricular fistula is a fistula between an atrium and a ventricle of the heart. ... Atrioventricular septal defect (AVSD) is characterized by a deficiency of the atrioventricular septum of the heart. ... Atrophy is the partial or complete wasting away of a part of the body. ... ATR-X is used to refer to Alpha-thalassemia X-Linked Mental Retardation, a condition caused by a mutuated gene. ... DISCLAIMER Please remember that Wikipedia is offered for informational use only. ...

Au-Az

• Auditory Perceptual Disorder
• Aughton syndrome
• Ausems Wittebol Post Hennekam syndrome
• Autoimmune hemolytic anemia
• Autoimmune hepatitis
• Autoimmune peripheral neuropathy
• Autoimmune polyendocrinopathy syndrome, type I
• Automysophobia
• Autonomic dysfunction
• Autonomic nervous system diseases
• Axial mesodermal dysplasia spectrum
• Axial osteomalacia
• Axial osteosclerosis
• Ayazi syndrome