A list of diseases in the English wikipedia. A disease is any abnormal condition of the body or mind that causes discomfort, dysfunction, or distress to the person affected 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. ... 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. ...

C

• C syndrome
• C1 esterase deficiency, (type 2 with ascites)

Ca

Cac-Cal

• Cacchi Ricci disease
• CACH syndrome
• Cacophobia
• Cafe au lait spots syndrome
• Caffey disease
• CAHMR syndrome
• Calcinosis cutis (see also CREST syndrome)
• Calciphylaxis
• Calculi
• Calderon Gonzalez Cantu syndrome
• Calloso genital dysplasia
• Callus disease
• Calpainopathy
• Calvarial hyperostosis

Cafe-au-lait spots are pigmented birthmarks. ... Calcinosis cutis (or cutaneous calcification) is a type of calcinosis wherein calcium deposits form in the skin. ... Scleroderma is a rare, chronic disease characterized by excessive deposits of collagen. ...

Cam-Can

• Camera Marugo -Cohen syndrome
• Camfak syndrome
• Campomelia Cumming type
• Camptobrachydactyly
• Camptocormism
• Camptodactyly fibrous tissue hyperplasia skeletal dysplasia
• Camptodactyly joint contractures facial skeletal dysplasia
• Camptodactyly overgrowth unusual facies
• Camptodactyly syndrome Guadalajara type 1
• Camptodactyly syndrome Guadalajara type 2
• Camptodactyly taurinuria
• Camptodactyly vertebral fusion
• Camptomelic syndrome
• Campylobacter infection
• Camurati Engelmann disease
• Canavan leukodystrophy
• Cancer
• Candidiasis familial chronic
• Candidiasis
• Canga's bead symptom
• Canine distemper
• Cantalamessa Baldini Ambrosi syndrome
• Cantu Sanchez Corona Fragoso syndrome
• Cantu Sanchez Corona Garcia syndrome
• Cantu Sanchez Corona Hernandes syndrome

Species see text Campylobacter is a genus of Gram-negative bacteria. ... When normal cells are damaged or old they undergo apoptosis; cancer cells, however, avoid apoptosis. ... Cangas bead symptom is a radiologic term used to define the irregular appearance of uterus and nodular structures in tuba uterina observed in patients with genital tuberculosis. ... Canine distemper is a disease affecting animals in the families Canidae, Mustelidae, Mephitidae, Procyonidae, and possibly Felidae (though not domestic cats; feline distemper or panleukopenia is a similar, but different virus exclusive to cats). ...

Cap

• Capillary leak syndrome with monoclonal gammopathy
• Capillary venous leptomeningeal angiomatosis
• Capos syndrome

Car

Cara-Carc

• Caratolo Cilio Pessagno syndrome
• Carbamoyl phosphate synthetase deficiency
• Carbamoyl-phosphate synthase I deficiency disease (ornithine carbamoyl phosphate deficiency)
• Carbohydrate deficient glycoprotein syndrome
• Carbon baby syndrome
• Carbonic anhydrase II deficiency
• Carcinoid syndrome
• Carcinoma of the vocal tract
• Carcinoma, squamous cell of head and neck
• Carcinoma, squamous cell
• Carcinophobia

// Basics: Carcinoid syndrome refers to the array of symptoms that occur secondary to carcinoid tumors. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ...

Card

Cardi

Cardia

• Cardiac and laterality defects
• Cardiac arrest
• Cardiac conduction defect, familial
• Cardiac diverticulum
• Cardiac hydatid cysts with intracavitary expansion
• Cardiac malformation
• Cardiac valvular dysplasia, X-linked

Cardio

• Cardioauditory syndrome of Sanchez- Cascos
• Cardioauditory syndrome
• Cardiofacial syndrome short limbs
• Cardiofaciocutaneous syndrome
• Cardiogenital syndrome
• Cardiomelic syndrome Stratton Koehler type
• Cardiomyopathy:
  • Arrhythmogenic right ventricular cardiomyopathy
  • Cardiomyopathic lentiginosis
  • Cardiomyopathy cataract hip spine disease
  • Cardiomyopathy diabetes deafness
  • Dilated cardiomyopathy: Cardiomyopathy dilated with conduction defect type 1, Cardiomyopathy dilated with conduction defect type 2, Cardiomyopathy, familial dilated
  • Cardiomyopathy due to anthracyclines
  • Cardiomyopathy hearing loss type t RNA lysine gene mutation
  • Hypertrophic cardiomyopathy: familial
  • Cardiomyopathy hypogonadism metabolic anomalies
  • Cardiomyopathy spherocytosis
  • Cardiomyopathy, fatal fetal, due to myocardial calcification
  • Cardiomyopathy, X linked, fatal infantile
  • Restrictive cardiomyopathy
• Cardiophobia
• Cardioskeletal myopathy-neutropenia
• Cardiospasm

Cardiofaciocutaneous Syndrome is an extremely rare and serious genetic condition. ... 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. ... Cardiomyopathy is the deterioration of the cardiac muscle of the heart wall. ... Hypertrophic cardiomyopathy, or HCM, is a disease of the myocardium (the muscle of the heart) in which a portion of the myocardium is hypertrophied (thickened) without any obvious cause. ... The English suffix -phobia is technically used to describe irrational, disabling fear as a mental disorder, and commonly misused to describe hatred of a particular thing or subject. ...

Care-Carr

• Carey Fineman Ziter syndrome
• Carnevale Canun Mendoza syndrome
• Carnevale Hernandez Castillo syndrome
• Carnevale Krajewska Fischetto syndrome
• Carney syndrome
• Carnitine palmitoyl transferase 1 deficiency
• Carnitine palmitoyl transferase 2 deficiency
• Carnitine palmitoyl transferase deficiency
• Carnitine transporter deficiency
• Carnitine-acylcarnitine translocase deficiency
• Carnophobia
• Carnosinase deficiency
• Carnosinemia
• Caroli disease
• Carotenemia
• Carpal deformity migrognathia microstomia
• Carpal tunnel syndrome
• Carpenter Hunter type
• Carpenter syndrome
• Carpo tarsal osteolysis recessive
• Carpotarsal osteochondromatosis
• Carrington syndrome

Primary carnitine deficiency is a condition that prevents the body from using fats for energy, particularly during periods without food. ... Carnitine-acylcarnitine translocase deficiency is a rare condition that prevents the body from converting long-chain fatty acids into energy, particularly during periods without food. ... Caroli disease is a rare congenital disease. ... Carotenemia is a condition that turns skin yellow from an intake of beta-carotene. ... Carpal tunnel syndrome is a disorder in which the median nerve is compressed at the wrist causing symptoms like tingling, pain, coldness, and sometimes weakness in parts of the hand. ...

Cart

• Cartilage hair hypoplasia like syndrome
• Cartilaginous neoplasms
• Cartwright Nelson Fryns syndrome

Cas

• Cassia Stocco Dos Santos syndrome
• Castleman's disease
• Castro Gago Pombo Novo syndrome

Castlemans disease is a rare disease of the lymphatic system, that causes the growth of benign tumors. ...

Cat

• Cat cry syndrome
• Cat Eye syndrome
• Cat Rodrigues syndrome
• Cat-scratch disease

5p- karyotype Cri du chat syndrome, also called deletion 5p syndrome, or 5p minus, is a rare genetic disorder due to a missing portion of chromosome 5. ... Cat Scratch Fever is also the title of a 1977 album by Ted Nugent. ...

Cata

• Catagelophobia
• Catapedaphobia
• Cataract,congenital ichthyosis
• Cataract aberrant oral frenula growth retardation
• Cataract anterior polar dominant
• Cataract ataxia deafness
• Cataract cardiomyopathy
• Cataract congenital autosomal dominant
• Cataract congenital dominant non nuclear
• Cataract congenital Volkmann type
• Cataract congenital with microphthalmia
• Cataract dental syndrome
• Cataract Hutterite type
• Cataract hypertrichosis mental retardation
• Cataract mental retardation hypogonadism
• Cataract microcornea syndrome
• Cataract microphthalmia septal defect
• Cataract skeletal anomalies
• Cataract, alopecia, sclerodactyly
• Cataract, congenital, with microcornea or slight microphthalmia
• Cataract, total congenital
• Cataract-glaucoma

Catc-Cate

• CATCH 22 syndrome
• Catecholamine hypertension
• Catel Manzke syndrome

22 q11 microdeletion syndrome is a birth defect caused by a genetic abnormality that occurs in approximately one in 700 births. ...

Cau-Cay

• Caudal appendage deafness
• Caudal duplication
• Caudal regression syndrome
• Causalgia
• Cavernous hemangioma
• Cavernous lymphangioma
• Cayler syndrome

Cc-Cd

• CCA syndrome
• Ccge syndrome
• CCHS
• CDG syndrome type 1A
• CDG syndrome type 1B
• CDG syndrome type 1C
• CDG syndrome type 2
• CDG syndrome type 3
• CDG syndrome type 4
• CDG syndrome
• CDK4 linked melanoma

CCHS may stand for: Christopher Columbus High School in Miami, Florida The Carleton County Historical Society The Cathedral Catholic High School part of the University of San Diego High School planned to open in 2005 This is a disambiguation page — a navigational aid which lists other pages that might otherwise... CDG syndrome is the abbreviation for Congenital Disorders of Glycosylation. CDG are rare inherited metabolic conditions which affects human development and physiology. ... CDG syndrome is the abbreviation for Congenital Disorders of Glycosylation. CDG are rare inherited metabolic conditions which affects human development and physiology. ...

Ce

Cec-Cep

• Cecato De lima Pinheiro syndrome
• Celiac disease epilepsy occipital calcifications
• Celiac sprue
• Cenani Lenz syndactylism
• Cennamo Gangemi syndrome
• Central core disease
• Central diabetes insipidus
• Central nervous system protozoal infections
• Central serous chorioretinopathy
• Central type neurofibromatosis
• Centromeric instability immunodeficiency syndrome
• Centronuclear myopathy, congenital
• Centrotemporal epilepsy
• Cephalopolysyndactyly

Coeliac disease (also termed non-tropical sprue, celiac disease and gluten intolerance) is an autoimmune disease characterised by chronic inflammation of the proximal portion of the small intestine caused by exposure to certain dietary gluten proteins. ... Cenani Lenz syndactylism (also known as Cenanis syndactyly) is a syndrome which consists of syndactyly (joined fingers) and brachymelia (disproportionate shortness of the limbs). ...

Cer

Cera

• Ceramidase deficiency
• Ceramide trihexosidosis
• Ceraunophobia

Cere

Cereb

Cerebe

• Cerebellar agenesis
• Cerebellar ataxia areflexia pes cavus optic atrophy
• Cerebellar ataxia ectodermal dysplasia
• Cerebellar ataxia infantile with progressive external ophthalmoplegia
• Cerebellar ataxia, dominant pure
• Cerebellar ataxia
• Cerebellar degeneration, subacute
• Cerebellar degeneration
• Cerebellar hypoplasia endosteal sclerosis
• Cerebellar hypoplasia tapetoretinal degeneration
• Cerebellar hypoplasia
• Cerebellar parenchymal degeneration
• Cerebelloolivary atrophy
• Cerebelloparenchymal disorder 3
• Cerebellum agenesis hydrocephaly

Cerebellar hypoplasia is a disorder found in cats and dogs in which the cerebellum is not completely mature at birth. ...

Cerebr

• Cerebral Amyloid Angiopathy, Familial
• Cerebral amyloid angiopathy
• Cerebral aneurysm
• Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
• Cerebral calcification cerebellar hypoplasia
• Cerebral calcifications opalescent teeth phosphaturia
• Cerebral cavernous malformation
• Cerebral cavernous malformations
• Cerebral gigantism jaw cysts
• Cerebral gigantism
• Cerebral malformations hypertrichosis claw hands
• Cerebral palsy
• Cerebral thrombosis -
• Cerebral ventricle neoplasm
• Cerebro facio articular syndrome
• Cerebro facio thoracic dysplasia
• Cerebro oculo dento auriculo skeletal syndrome
• Cerebro oculo genital syndrome
• Cerebro oculo skeleto renal syndrome
• Cerebro reno digital syndrome
• Cerebroarthrodigital syndrome
• Cerebro-costo-mandibular syndrome
• Cerebro-oculo-facio-skeletal syndrome
• Cerebroretinal vasculopathy

A cerebral or brain aneurysm is a cerebrovascular disorder in which weakness in the wall of a cerebral artery or vein causes a localized dilation or ballooning of the blood vessel. ... Cerebral cavernous malformations (CCM), also known as cavernous angioma, cavernous haemangioma, and cavernoma, is a vascular disorder of the central nervous system that may appear either sporadically or exhibit autosomal dominant inheritance. ... Cerebral palsy or CP is a group of permanent disorders associated with developmental brain injuries that occur during fetal development, birth, or shortly after birth. ...

Cero-Cerv

• Ceroid lipofuscinose, neuronal 1, infantile
• Ceroid lipofuscinose, neuronal 2, late infantile
• Ceroid lipofuscinose, neuronal 3, juvenile
• Ceroid lipofuscinose, neuronal 4, adult type
• Ceroid lipofuscinose, neuronal 5, late infantile,
• Ceroid lipofuscinose, neuronal 6, late infantile
• Ceroid lipofuscinose, neuronal
• Ceroid lipofuscinosis, neuronal 4
• Cervical cancer
• Cervical hypertrichosis neuropathy
• Cervical hypertrichosis peripheral neuropathy
• Cervical ribs sprengel anomaly polydactyly
• Cervical vertebral fusion
• Cervicooculoacoustic syndrome

Cervical cancer is a malignancy of the cervix. ...

Ch

Cha

Chag-Chao

• Chagas disease
• Chalazion
• Chanarin disease
• Chanarin Dorfman syndrome ichthyosis
• Chancroid
• Chandler's syndrome
• Chands syndrome
• Chang Davidson Carlson syndrome
• Chaotic atrial tachycardia

A chalazion is a cyst in the eyelid that is caused by inflammation of the meibomian gland, usually on the upper eyelid. ... Binomial name Haemophilus ducreyi A chancroid is an STD characterized by painful sores on the genitalia. ...

Char

• Char syndrome

Charc

Charco

Charcot Charcot d

• Charcot disease

Charcot Marie Tooth disease

• Charcot Marie tooth disease deafness dominant type
• Charcot Marie tooth disease deafness mental retardation
• Charcot Marie Tooth disease deafness recessive type
• Charcot Marie Tooth type 1 aplasia cutis congenita
• Charcot-Marie-Tooth disease type 1A
• Charcot-Marie-Tooth disease type 1B
• Charcot-Marie-Tooth disease type 1C
• Charcot-Marie-Tooth disease type 2A
• Charcot-Marie-Tooth disease type 2B1
• Charcot-Marie-Tooth disease type 2B2
• Charcot-Marie-Tooth disease type 2C
• Charcot-Marie-Tooth disease type 2D
• Charcot-Marie-Tooth disease type 4A
• Charcot-Marie-Tooth disease type 4B
• Charcot-Marie-Tooth disease with ptosis and parkinsonism
• Charcot-Marie-Tooth disease, intermediate form
• Charcot-Marie-Tooth disease, neuronal, type A
• Charcot-Marie-Tooth disease, neuronal, type B
• Charcot-Marie-Tooth disease, neuronal, type D
• Charcot-Marie-Tooth disease, X-linked type 2, recessive
• Charcot-Marie-Tooth disease, X-linked type 3, recessive
• Charcot-Marie-Tooth disease
• Charcot-Marie-Tooth peroneal muscular atrophy, X-linked

The foot of a person with Charcot-Marie-Tooth. ...

Charg-Charl

• CHARGE Association
• Charles' Disease
• Charlie M syndrome

Chav

• Chavany-Brunhes syndrome

Che

• Chediak-Higashi syndrome
• Cheilitis glandularis
• Chemke Oliver Mallek syndrome
• Chemodectoma
• Chemophobia
• Chen Kung Ho Kaufman Mcalister syndrome
• Cherubism
• Cherubism

Chédiak-Higashi syndrome is a rare childhood autosomal recessive disorder that affects multiple systems of the body. ...

Chi-Chl

• Chiari type 1 malformation
• Chiari-Frommel syndrome
• Chickenpox
• Chikungunya
• CHILD syndrome ichthyosis
• Childhood disintegrative disorder
• Childhood pustular psoriasis
• Chionophobia
• Chiraptophobia
• Chirophobia
• Chitayat Haj Chahine syndrome
• Chitayat Meunier Hodgkinson syndrome
• Chitayat Moore Del Bigio syndrome
• Chitty Hall Baraitser syndrome
• Chitty Hall Webb syndrome
• Chlamydia trachomatis
• Chlamydia
• Chlamydial and Gonococcal Conjunctivitis

Chicken pox, also spelled chickenpox, is a common childhood disease caused by the varicella-zoster virus (VZV), also known as human herpes virus 3 (HHV-3), one of the eight herpesviruses known to affect humans. ... Chikungunya is a rare form of viral fever caused by an alphavirus that is spread by mosquito bites from the Aedes aegypti mosquito. ... Childhood disintegrative disorder (CDD) is a rare condition characterized by late onset (>3 years of age) of developmental delays in language, social function, and motor skills. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... Binomial name Chlamydia trachomatis Busacca, 1935 Chlamydia trachomatis is a gram-negative obligate intracellular bacterium. ... Chlamydia is currently one of the most common sexually transmitted disease — about 4 million cases of chlamydia occur in the USA each year. ...

Cho

Choa-Chol

• Choanal atresia deafness cardiac defects dysmorphia
• Cholangiocarcinoma
• Cholangitis, primary sclerosing
• Cholecystitis
• Choledochal cyst, hand malformation
• Cholemia, familial
• Cholera
• Cholerophobia
• Cholestasis pigmentary retinopathy cleft palate
• Cholestasis, progressive familial intrahepatic 1
• Cholestasis, progressive familial intrahepatic 2
• Cholestasis, progressive familial intrahepatic 3
• Cholestasis, progressive familial intrahepatic
• Cholestasis
• Cholestatic jaundice renal tubular insufficiency
• Cholesterol ester storage disease
• Cholesterol esterification disorder
• Cholesterol pneumonia

Cholangiocarcinoma is an adenocarcinoma of the biliary duct system. ... Cholecystitis is inflammation of the gallbladder. ... Distribution of cholera Cholera (also called Asiatic cholera) is an infectious disease of the gastrointestinal tract caused by the Vibrio cholerae bacterium. ...

Chon

• Chondroblastoma (benign)
• Chondrocalcinosis familial articular
• Chondrocalcinosis
• Chondrodysplasia lethal recessive
• Chondrodysplasia pseudohermaphrodism syndrome
• Chondrodysplasia punctata 1, x-linked recessive
• Chondrodysplasia punctata with steroid sulfatase deficiency
• Chondrodysplasia punctata, brachytelephalangic
• Chondrodysplasia punctata, Sheffield type
• Chondrodysplasia punctata
• Chondrodysplasia situs inversus imperforate anus polydactyly
• Chondrodysplasia, Grebe type
• Chondrodystrophy
• Chondroectodermal dysplasia
• Chondroma (benign)
• Chondromalacia
• Chondromatosis (benign)
• Chondrosarcoma (malignant)
• Chondrysplasia punctata, humero-metacarpal type

Categories: Stub ... A chondrosarcoma is a cancer of the cartilage. ...

Chor

• Chordoma
• Chorea acanthocytosis
• Chorea familial benign
• Chorea minor
• Chorea
• Choreoacanthocytosis amyotrophic
• Choreoathetosis familial paroxysmal
• Choriocarcinoma
• Chorioretinitis
• Chorioretinopathy dominant form microcephaly
• Choroid plexus cyst
• Choroid Plexus neoplasms
• Choroidal atrophy alopecia
• Choroideremia hypopituitarism
• Choroideremia
• Choroiditis, serpiginous
• Choroiditis
• Choroido cerebral calcification syndrome infantile
• Chorophobia

Chorea acanthocytosis is a rare hereditary disease caused by a mutation of the gene that directs structural proteins in red blood cells. ... Chorea is the occurrence of continuous rapid, jerky, involuntary movements that may involve the face and limb and result in an inability to maintain a posture. ... Choriocarcinoma is a rare cancer of the placenta, curable by chemotherapy. ... In medicine, Chorioretinitis is an inflammation of the choroid and retina of the eye. ... The brain contains pockets or spaces called ventricles with a spongy layer of cells and blood vessels called the choroid plexus. ...

Chr

Chri

• Christian Demyer Franken syndrome
• Christian Johnson Angenieta syndrome
• Christian syndrome
• Christianson Fourie syndrome
• Christmas disease

Haemophilia B (also spelled Hemophilia B or Hæmophilia B) is a blood clotting disorder caused by a mutation of the Factor IX gene. ...

Chro

Chrom

Chromo

Chromom-Chromop

• Chromomycosis
• Chromophobe renal carcinoma
• Chromophobia

Chromos Chromosoma The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ...

• Chromosomal triplication

Chromosome Chromosome 1

• Chromosome 1 ring
• Chromosome 1, 1p36 deletion syndrome
• Chromosome 1, deletion q21 q25
• Chromosome 1, duplication 1p21 p32
• Chromosome 1, monosomy 1p
• Chromosome 1, monosomy 1p22 p13
• Chromosome 1, monosomy 1p31 p22
• Chromosome 1, monosomy 1p32
• Chromosome 1, monosomy 1p34 p32
• Chromosome 1, monosomy 1q25 q32
• Chromosome 1, monosomy 1q32 q42
• Chromosome 1, monosomy 1q4
• Chromosome 1, q42 11 q42 12 duplication
• Chromosome 1, trisomy 1q32 qter
• Chromosome 1, trisomy 1q42 qter
• Chromosome 1, uniparental disomy 1q12 q21

Chromosome 10-Chromosome 12

• Chromosome 10 ring
• Chromosome 10, distal trisomy 10q
• Chromosome 10, monosomy 10p
• Chromosome 10, monosomy 10q
• Chromosome 10, trisomy 10p
• Chromosome 10, trisomy 10pter p13
• Chromosome 10, trisomy 10q
• Chromosome 10, uniparental disomy of
• Chromosome 10p terminal deletion syndrome
• Chromosome 11, deletion 11p
• Chromosome 11, partial trisomy 11q
• Chromosome 11-14 translocation
• Chromosome 11p, partial deletion
• Chromosome 11q partial deletion
• Chromosome 11q trisomy
• Chromosome 12 ring
• Chromosome 12, 12p trisomy
• Chromosome 12, trisomy 12q
• Chromosome 12p deletion
• Chromosome 12p partial deletion

Chromosome 13-Chromosome 15

• Chromosome 13 duplication
• Chromosome 13 ring
• Chromosome 13, partial monosomy 13q
• Chromosome 13p duplication
• Chromosome 13q deletion
• Chromosome 13q trisomy
• Chromosome 13q-mosaicism
• Chromosome 14 ring
• Chromosome 14 trisomy
• Chromosome 14, deletion 14q, partial duplication 14p
• Chromosome 14, trisomy mosaic
• Chromosome 14q, partial deletions
• Chromosome 14q, proximal duplication
• Chromosome 14q, terminal deletion
• Chromosome 14q, terminal duplication
• Chromosome 15 ring
• Chromosome 15, distal trisomy 15q
• Chromosome 15, trisomy mosaicism
• Chromosome 15q, partial deletion
• Chromosome 15q, tetrasomy
• Chromosome 15q, trisomy

Chromosome 16-Chromosome 1q Chromosome 15q partial deletion is an extremely rare genetic disorder, caused by a chromosomal aberration in which one of the long (q) arms of human chromosome 15 is deleted. ... Chromosome 15q trisomy is an extremely rare genetic disorder, caused by a chromosomal aberration in which there is an excess copy of the long (q) arm of human chromosome 15. ...

• Chromosome 16, trisomy 16p
• Chromosome 16, trisomy 16q
• Chromosome 16, trisomy
• Chromosome 16, uniparental disomy
• Chromosome 17 trisomy
• Chromosome 17 deletion
• Chromosome 17 ring
• Chromosome 17, deletion 17q23 q24
• Chromosome 17, trisomy 17p
• Chromosome 17, trisomy 17p11 2
• Chromosome 17, trisomy 17q22
• Chromosome 18 long arm deletion syndrome
• Chromosome 18 mosaic monosomy
• Chromosome 18 ring
• Chromosome 18, deletion 18q23
• Chromosome 18, monosomy 18p
• Chromosome 18, tetrasomy 18p
• Chromosome 18, trisomy 18p
• Chromosome 18, trisomy 18q
• Chromosome 18, trisomy
• Chromosome 19 ring
• Chromosome 19, trisomy 19q
• Chromosome 1q, duplication 1q12 q21

Chromosome 2

• Chromosome 2, monosomy 2p22
• Chromosome 2, monosomy 2pter p24
• Chromosome 2, monosomy 2q
• Chromosome 2, monosomy 2q24
• Chromosome 2, monosomy 2q37
• Chromosome 2, trisomy 2p
• Chromosome 2, Trisomy 2p13 p21
• Chromosome 2, trisomy 2pter p24
• Chromosome 2, trisomy 2q
• Chromosome 2, trisomy 2q37

Chromosome 20-Chromosome 22

• Chromosome 20 ring
• Chromosome 20, deletion 20p
• Chromosome 20, duplication 20p
• Chromosome 20, trisomy
• Chromosome 21 monosomy
• Chromosome 21 ring
• Chromosome 21, monosomy 21q22
• Chromosome 21, tetrasomy 21q
• Chromosome 21, uniparental disomy of
• Chromosome 22 ring
• Chromosome 22 trisomy mosaic
• Chromosome 22, microdeletion 22 q11
• Chromosome 22, monosome mosaic
• Chromosome 22, trisomy q11 q13
• Chromosome 22, trisomy

Chromosome 3 This article needs to be cleaned up to conform to a higher standard of quality. ...

• Chromosome 3 duplication syndrome
• Chromosome 3, monosomy 3p
• Chromosome 3, monosomy 3p14 p11
• Chromosome 3, monosomy 3p2
• Chromosome 3, monosomy 3p25
• Chromosome 3, monosomy 3q13
• Chromosome 3, monosomy 3q21 23
• Chromosome 3, monosomy 3q27
• Chromosome 3, trisomy 3p
• Chromosome 3, trisomy 3p25
• Chromosome 3, trisomy 3q
• Chromosome 3, trisomy 3q13 2 q25
• Chromosome 3, Trisomy 3q2

Chromosome 4-Chromosome 5

• Chromosome 4 ring
• Chromosome 4 short arm deletion
• Chromosome 4, monosomy 4p14 p16
• Chromosome 4, monosomy 4q
• Chromosome 4, monosomy 4q32
• Chromosome 4, monosomy distal 4q
• Chromosome 4, partial trisomy distal 4q
• Chromosome 4, Trisomy 4p
• Chromosome 4, trisomy 4q
• Chromosome 4, trisomy 4q21
• Chromosome 4, trisomy 4q25 qter
• Chromosome 5, monosomy 5q35
• Chromosome 5, trisomy 5p
• Chromosome 5, trisomy 5pter p13 3
• Chromosome 5, trisomy 5q
• Chromosome 5, uniparental disomy

Chromosome 6-Chromosome 7

• Chromosome 6 ring
• Chromosome 6, deletion 6q13 q15
• Chromosome 6, monosomy 6p23
• Chromosome 6, monosomy 6q
• Chromosome 6, monosomy 6q1
• Chromosome 6, monosomy 6q2
• Chromosome 6, partial trisomy 6q
• Chromosome 6, trisomy 6p
• Chromosome 6, trisomy 6q
• Chromosome 7 ring
• Chromosome 7, monosomy 7q2
• Chromosome 7, monosomy 7q21
• Chromosome 7, monosomy 7q3
• Chromosome 7, monosomy
• Chromosome 7, partial monosomy 7p
• Chromosome 7, trisomy 7p
• Chromosome 7, trisomy 7p13 p12 2
• Chromosome 7, trisomy 7q
• Chromosome 7, trisomy mosaic

Chromosome 8-Chromosome 9

• Chromosome 8 deletion
• Chromosome 8 ring
• Chromosome 8, monosomy 8p
• Chromosome 8, monosomy 8p2
• Chromosome 8, monosomy 8p23 1
• Chromosome 8, monosomy 8q
• Chromosome 8, mosaic trisomy
• Chromosome 8, partial trisomy
• Chromosome 8, trisomy 8p
• Chromosome 8, trisomy 8q
• Chromosome 8, trisomy
• Chromosome 9 inversion or duplication
• Chromosome 9 Ring
• Chromosome 9, duplication 9q21
• Chromosome 9, monosomy 9p
• Chromosome 9, partial monosomy 9p
• Chromosome 9, partial trisomy 9p
• Chromosome 9, tetrasomy 9p
• Chromosome 9, trisomy 9q
• Chromosome 9, trisomy 9q32
• Chromosome 9, trisomy mosaic
• Chromosome 9, trisomy

Chromosomes

• Chromosomes 1 and 2, monosomy 2q duplication 1p

Chron

• Chronic berylliosis
• Chronic demyelinizing neuropathy with IgM monoclonal
• Chronic erosive gastritis
• Chronic fatigue immune dysfunction syndrome
• Chronic fatigue syndrome
• Chronic granulomatous disease
• Chronic hiccup
• Chronic inflammatory demyelinating polyneuropathy
• Chronic lymphocytic leukemia
• Chronic myelogenous leukemia
• Chronic myelomonocytic leukemia
• Chronic necrotizing vasculitis
• Chronic neutropenia
• Chronic polyradiculoneuritis
• Chronic recurrent multifocal osteomyelitis
• Chronic renal failure
• Chronic spasmodic dysphonia
• Chronic, infantile, neurological, cutaneous, articular syndrome
• Chronomentrophobia

Chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis (ME), post-viral fatigue syndrome (PVFS) and various other names, is a disorder of the central nervous system (CNS) characterized by a number of features, the most common and notable one being severe fatigue, usually made worse by even modest exertion. ... In medicine (genetics and pediatrics) chronic granulomatous disease (CGD) is a hereditary disease where neutrophil granulocytes are unable to destroy ingested pathogens. ... Chronic lymphocytic leukemia, or CLL, is a cancer in which too many lymphocytes (a type of white blood cells) are produced. ... Chronic myelogenous leukemia (or CML) is a form of chronic leukemia characterised by increased production of myeloid cells in the bone marrow. ...

Chu-Chy

• Chudley Lowry Hoar syndrome
• Chudley Rozdilsky syndrome
• Chudley-Mccullough syndrome
• Churg-Strauss syndrome
• Chylous ascites

Churg-Strauss syndrome (also known as allergic granulomatosis) is a form of vasculitis due to autoimmunity, leading to necrosis. ...

Ci

• Cicatricial pemphigoid
• Ciguatera fish poisoning
• Ciliary discoordination, due to random ciliary orientation
• Ciliary dyskinesia, due to transposition of ciliary microtubules
• Ciliary dyskinesia-bronchiectasis
• Cilliers Beighton syndrome
• Cinchonism
• Circumscribed cutaneous aplasia of the vertex
• Circumscribed disseminated keratosis Jadassohn Lew type
• Citrullinemia

Ciguatera fish poisoning (or ciguatera) is an illness caused by eating fish that contain toxins produced by a marine microalgae called Gambierdiscus toxicus. ... Cinchonism or quinism is a pathological condition in humans caused by an overdose of quinine or its natural source, cinchona bark. ... Citrullinemia s an inherited disorder that causes ammonia and other toxic substances to accumulate in the blood. ...

Cl

Cla

• Clarkson disease
• Clayton Smith Donnai syndrome

Cle

Clef

Cleft

Cleft h-Cleft l

• Cleft hand absent tibia
• Cleft lip and palate malrotation cardiopathy
• Cleft lip and/or palate with mucous cysts of lower
• Cleft lip palate abnormal thumbs microcephaly
• Cleft lip palate deafness sacral lipoma
• Cleft lip palate dysmorphism Kumar type
• Cleft lip palate ectrodactyly
• Cleft lip palate incisor and finger anomalies
• Cleft lip palate mental retardation corneal opacity
• Cleft lip palate oligodontia syndactyly pili torti
• Cleft lip palate pituitary deficiency
• Cleft lip palate-tetraphocomelia
• Cleft lip with or without cleft palate
• Cleft lip
• Cleft lower lip cleft lateral canthi chorioretinal

Cleft p-Cleft u

• Cleft palate cardiac defect ectrodactyly
• Cleft palate colobomata radial synostosis deafness
• Cleft palate heart disease polydactyly absent tibia
• Cleft palate lateral synechia syndrome
• Cleft palate short stature vertebral anomalies
• Cleft palate stapes fixation oligodontia
• Cleft palate X linked
• Cleft palate
• Cleft tongue syndrome
• Cleft upper lip median cutaneous polyps

Clefti

• Clefting ectropion conical teeth

Clei

• Cleidocranial dysplasia micrognathia absent thumbs
• Cleidocranial dysplasia
• Cleisiophobia

Cli-Clu

• Climacophobia
• Clinophobia
• Cloacal exstrophy
• Clouston syndrome
• Cloverleaf skull bone dysplasia
• Cloverleaf skull micromelia thoracic dysplasia
• Cluster headache

Climacophobia is the fear of walking up or falling down stairs. ... Clinophobia is the fear of going to bed. ... Cloacal exstrophy is a severe birth defect wherein much of the abdominal organs (the bladder and intestines) are exposed. ... Cluster headaches are rare headaches that occur in groups or clusters. ...

Cm

• CMV antenatal infection

Co

Coa-Cof

• Coach syndrome
• Coal worker's pneumoconiosis
• Coarctation of aorta dominant
• Coarse face hypotonia constipation
• Coats disease
• Cocaine antenatal infection
• Cocaine fetopathy
• Coccidioidomycosis
• Cochin Jewish Disorder
• Cockayne syndrome type 1
• Cockayne syndrome type 2
• Cockayne syndrome type 3
• Cockayne's syndrome
• Codas syndrome
• Coenzyme Q cytochrome c reductase deficiency of
• Coffin-Lowry syndrome
• Coffin-Siris syndrome
• COFS syndrome

Coffin-Lowry syndrome is a condition associated with mental retardation and delayed development, characteristic facial features, and skeletal abnormalities. ...

Cog-Coh

• Cogan-Reese syndrome
• Cogan's syndrome
• Cohen Hayden syndrome
• Cohen Lockood Wyborney syndrome
• Cohen syndrome

Col

Cola-Coll

• Colavita Kozlowski syndrome
• Cold agglutination syndrome
• Cold agglutinin disease
• Cold antibody hemolytic anemia
• Cold contact urticaria
• Cold urticaria
• Cole carpenter syndrome
• Coleman Randall syndrome
• Colitis
• Collagen disorder
• Collagenous colitis
• Collins Pope syndrome
• Collins Sakati syndrome

Colitis has been confused with Crohns disease in the past. ...

Colo-Colv

• Coloboma chorioretinal cerebellar vermis aplasia
• Coloboma hair abnormality
• Coloboma of choroid and retina
• Coloboma of eye lens
• Coloboma of iris
• Coloboma of lens ala nasi
• Coloboma of macula type B brachydactyly
• Coloboma of macula
• Coloboma of optic nerve
• Coloboma of optic papilla
• Coloboma porencephaly hydronephrosis
• Coloboma uveal with cleft lip palate and mental retardation
• Coloboma, ocular
• Colobomata unilobar lung heart defect
• Colobomatous microphthalmia heart disease hearing
• Colobomatous microphthalmia
• Colon cancer, familial nonpolyposis
• Colonic atresia
• Colonic malakoplakia
• Color blindness
• Colorado tick fever
• Colver Steer Godman syndrome

Color blindness in humans is the inability to perceive differences between some or all colors that other people can distinguish. ... In medicine Colorado Tick Fever is an illness caused by a virus carried by small mammals, such as ground squirrels, porcupines, and chipmunks, and by ticks. ...

Com

• Combarros Calleja Leno syndrome
• Combined hyperlipidemia, familial
• Common cold
• Common mesentery
• Common variable immunodeficiency
• Compartment syndrome
• Complement component 2 deficiency
• Complement component receptor 1
• Complete atrioventricular canal
• Complex 1 mitochondrial respiratory chain deficiency
• Complex 2 mitochondrial respiratory chain deficiency
• Complex 3 mitochondrial respiratory chain deficiency
• Complex 4 mitochondrial respiratory chain deficiency
• Complex 5 mitochondrial respiratory chain deficiency

In medicine, combined hyperlipidemia (or -aemia) is a commonly occurring form of hypercholesterolemia (elevated cholesterol levels) characterised by increased LDL and triglyceride concentrations, often accompanied by decreased HDL. On lipoprotein electrophoresis (a test now rarely performed) is shows as a hyperlipoproteinemia type IIB. The elevated triglyceride levels (>5 mmol/l... The common cold is a mild viral infectious disease of the nose and throat; the upper respiratory system. ... On the human body, the limbs can be divide into segments, such as the arm and the forearm of the upper limb, and the thigh and the leg of the lower limb. ...

Con

Cond-Cone

• Conductive deafness malformed external ear
• Conductive hearing loss
• Condyloma acuminatum
• Condyloma
• Cone dystrophy
• Cone rod dystrophy amelogenesis imperfecta
• Cone rod dystrophy

Conductive hearing loss is a failure in the efficient conduction of sound waves through the outer ear, typanic membrane (eardrum) or middle ears (ossicles). ... Genital warts (or condyloma) is a very contagious sexually transmitted disease. ... Genital warts or (or condyloma) is a very contagious sexually transmitted disease. ... Cone cells are photoreceptors responsible for both central and color vision. ...

Cong

Conge

Congen

Congenital a-Congenital b

• Congenital absence of the uterus and vagina
• Congenital adrenal hyperplasia type 1
• Congenital adrenal hyperplasia type 2
• Congenital adrenal hyperplasia type 3
• Congenital adrenal hyperplasia type 4
• Congenital adrenal hyperplasia type 5
• Congenital adrenal hyperplasia
• Congenital afibrinogenemia
• Congenital alopecia X linked
• Congenital amputation
• Congenital aneurysms of the great vessels
• Congenital antithrombin III deficiency
• Congenital aplastic anemia
• Congenital arteriovenous shunt
• Congenital articular rigidity
• Congenital benign spinal muscular atrophy dominant
• Congenital brain disorder
• Congenital bronchobiliary fistula

Congenital c-Congenital g 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 cardiovascular disorder
• Congenital cardiovascular malformations
• Congenital cardiovascular shunt
• Congenital constricting band
• Congenital contractual arachnodactyly
• Congenital contractures
• Congenital craniosynostosis maternal hyperthyroiditis
• Congenital cystic adenomatoid malformation
• Congenital cystic eye multiple ocular and intracranial anomalies
• Congenital cytomegalovirus
• Congenital deafness
• Congenital diaphragmatic hernia
• Congenital erythropoietic porphyria
• Congenital facial diplegia
• Congenital fiber type disproportion
• Congenital gastrointestinal disorder
• Congenital generalized fibromatosis
• Congenital giant megaureter

Congenital h-Congenital l Congenital Diaphragmatic Hernia (CDH) is a congenital abnormality that is often life-threatening. ... The porphyrias are inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). ...

• Congenital heart block
• Congenital heart disease ptosis hypodontia craniostosis
• Congenital heart disease radio ulnar synostosis mental retardation
• Congenital heart disorder
• Congenital heart septum defect
• Congenital hemidysplasia with ichtyosiform erythroderma and limbs defects
• Congenital hemolytic anemia
• Congenital hepatic fibrosis
• Congenital hepatic porphyria
• Congenital herpes simplex
• Congenital hypomyelination neuropathy
• Congenital hypothyroidism
• Congenital hypotrichosis milia
• Congenital ichthyosis, microcephalus, quadriplegia
• Congenital ichthyosis
• Congenital ichtyosiform erythroderma
• Congenital kidney disorder
• Congenital lobar emphysema

Congenital m-Congenital s Congenital hypothyroidism is a condition of thyroid hormone deficiency present at birth. ...

• Congenital megacolon
• Congenital megalo-ureter
• Congenital mesoblastic nephroma
• Congenital microvillous atrophy
• Congenital mitral malformation
• Congenital mitral stenosis
• Congenital mixovirus
• Congenital mumps
• Congenital muscular dystrophy syringomyelia
• Congenital myopathy
• Congenital nephrotic syndrome, Finnish type
• Congenital nonhemolytic jaundice
• Congenital rubella
• Congenital short bowel
• Congenital short femur
• Congenital skeletal disorder
• Congenital skin disorder
• Congenital spherocytic anemia
• Congenital spherocytic hemolytic anemia
• Congenital stenosis of cervical medullary canal
• Congenital sucrose isomaltose malabsorption
• Congenital syphilis

Congenital t-Congenital v

• Congenital toxoplasmosis
• Congenital unilateral pulmonary hypoplasia
• Congenital vagal hyperreflexivity
• Congenital varicella syndrome

Conges

• Congestive heart disease

Congestive heart failure (CHF) (also called Congestive Cardiac Failure and heart failure) is the inability of the heart to pump a sufficient amount of blood throughout the body, or requiring elevated filling pressures in order to pump effectively. ...

Conju

• Conjunctivitis ligneous
• Conjunctivitis with Pseudomembrane
• Conjunctivitis

Conn-Conv

• Connective tissue dysplasia Spellacy type
• Connexin 26 anomaly
• Conn's syndrome
• Conotruncal heart malformations
• Conradi-Hünermann syndrome
• Constitutional growth delay
• Constrictive bronchiolitis
• Continuous muscle fiber activity hereditary
• Continuous spike-wave during slow sleep syndrome
• Contractural arachnodactyly
• Contractures ectodermal dysplasia cleft lip palate
• Contractures hyperkeratosis lethal
• Contractures of feet-muscle atrophy-oculomotor apraxia
• Conversion disorder
• Convulsions benign familial neonatal dominant form
• Convulsions benign familial neonatal

Conns syndrome is overproduction of the mineralocorticoid hormone aldosterone by the adrenal glands. ... Definition Constitutional growth delay (CGD) is a term describing a temporary delay in the skeletal growth and height of a child with no other physical abnormalities causing the delay. ... Conversion disorders, categorised under the heading of Somatoform Disorders in both DSM IV and ICD 10 have an historical heritage in the classical descriptions of hysteria as presented by, for example, Sigmund Freud. ...

Coo-Cop

• Cooks syndrome
• Cooley's anemia
• Copper deficiency familial benign
• Copper transport disease
• Coprastasophobia
• Coprophobia
• Coproporhyria

The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... The porphyrias are inherited or acquired disorders of certain enzymes in the heme biosynthetic pathway (also called porphyrin pathway). ...

Cor

• Cor biloculare
• Cor triatriatum

Corm-Coro

• Cormier Rustin Munnich syndrome
• Corneal anesthesia deafness mental retardation
• Corneal cerebellar syndrome
• Corneal crystals myopathy neuropathy
• Corneal dystrophy epithelial short stature
• Corneal dystrophy ichthyosis microcephaly mental retardation
• Corneal dystrophy perceptive deafness
• Corneal dystrophy pigmentary anomaly malabsorption
• Corneal dystrophy
• Corneal endothelium dystrophy
• Cornelia de Lange syndrome
• Corneodermatoosseous syndrome
• Coronal synostosis syndactyly jejunal atresia
• Coronaro-cardiac fistula
• Coronary arteries congenital malformation
• Coronary artery aneurysm
• Coronary heart disease

Coronary heart disease (CHD), also called coronary artery disease (CAD) and atherosclerotic heart disease, is the end result of the accumulation of atheromatous plaques within the walls of the arteries that supply the myocardium (the muscle of the heart). ...

Corp-Cort

• Corpus callosum agenesis double urinary collecting
• Corpus callosum agenesis neuronopathy
• Corpus callosum agenesis of blepharophimosis Robin type
• Corpus callosum agenesis of with chorioretinal abnormalities
• Corpus callosum agenesis polysyndactyly
• Corpus callosum agenesis
• Corpus callosum dysgenesis cleft spasm
• Corpus callosum dysgenesis hypopituitarism
• Corpus callosum dysgenesis X linked recessive
• Corrected transposition
• Corsello Opitz syndrome
• Cortada Koussef Matsumoto syndrome
• Cortes Lacassie syndrome
• Cortical blindness mental retardation polydactyly
• Cortical degeneration of the cerebellum parenchymatous
• cortical dysplasia
• Cortical hyperostosis syndactyly
• Corticobasal degeneration

Cortical dysplasia is a benign tumor which occurs when the infant brain is developing in the womb, occasionally the neurons will develop larger than normal in certain areas. ...

Cos-Cox

• Costello syndrome
• Costochondritis (otherwise Costal chondritis)
• Costocoracoid ligament congenitally short
• Cote Adamopoulos Pantelakis syndrome
• Cote Katsantoni syndrome
• Cousin Walbraum Cegarra syndrome
• Covesdem syndrome
• Cowchock Wapner Kurtz syndrome
• Cowden's disease
• Cowpox
• Coxoauricular syndrome

A benign inflammation of the ligaments connecting to the sternum or ribs, Tietzes Syndrome is most common among patients who have had thoracic surgery. ... A benign inflammation of the ligaments connecting to the sternum or ribs, Tietzes Syndrome is most common among patients who have had thoracic surgery. ... Cowpox is a disease of the skin caused by a virus (Cowpox virus) that is related to the Vaccinia virus. ...

Cr

Cra

Cram

• Cramer Niederdellmann syndrome
• Cramp-fasciculations syndrome

Cran

Crand-Crane

• Crandall syndrome
• Crane-Heise syndrome

Crani

Cranio

• Cranio osteoarthropathy

Cranioa-Craniom

• Cranioacrofacial syndrome
• Craniodiaphyseal dysplasia
• Craniodigital syndrome mental retardation
• Cranioectodermal dysplasia
• Craniofacial and osseous defects mental retardation
• Craniofacial and skeletal defects
• Craniofacial deafness hand syndrome
• Craniofacial dysostosis arthrogryposis progeroid appearance
• Craniofacial dysostosis
• Craniofacial dysynostosis
• Craniofaciocardioskeletal syndrome
• Craniofaciocervical osteoglyphic dysplasia
• Craniofrontonasal dysplasia
• Craniofrontonasal syndrome Teebi type
• Craniometaphyseal dysplasia dominant type
• Craniometaphyseal dysplasia recessive type
• Craniomicromelic syndrome

Cranios-Craniot Craniodiaphyseal dysplasia (also known as lionitis) is a disease that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy. ...

• Craniostenosis cataract
• Craniostenosis with congenital heart disease mental retardation
• Craniostenosis
• Craniosynostosis alopecia brain defect
• Craniosynostosis arthrogryposis cleft palate
• Craniosynostosis autosomal dominant
• Craniosynostosis cleft lip palate arthrogryposis
• Craniosynostosis contractures cleft
• Craniosynostosis exostoses nevus epibulbar dermoid
• Craniosynostosis fibular aplasia
• Craniosynostosis Fontaine type
• Craniosynostosis Maroteaux Fonfria type
• Craniosynostosis mental retardation clefting syndrome
• Craniosynostosis mental retardation heart defects
• Craniosynostosis Philadelphia type
• Craniosynostosis radial aplasia syndrome
• Craniosynostosis synostoses hypertensive nephropathy
• Craniosynostosis Warman type
• Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus
• Craniosynostosis
• Craniotelencephalic dysplasia

Craniostenoses are a group of cephalic disorders in which the plates of the cranium in children fuse prematurely, resulting in deformities of the skull. ... It is the medical condition where the bones in the head fuse prematurely in a growing infant. ...

Craw

• Crawfurd syndrome

Cre-Cro

• Creatine deficiency
• Creeping disease
• CREST syndrome (Calcinosis Raynaud's Esophagus Sclerodactyly Telangiectasia)
• Cretinism athyreotic
• Cretinism
• Creutzfeldt-Jakob disease
• Cri du chat syndrome
• Crigler Najjar syndrome type I
• Crisponi syndrome
• Criss cross syndrome
• Criswick-Schepens syndrome
• Crohn's disease of the esophagus
• Crohn's disease
• Crome syndrome
• Cronkhite-Canada disease
• Crossed polydactyly type 1
• Crossed polysyndactyly
• Crow-Fukase syndrome

Scleroderma is a rare, chronic disease characterized by excessive deposits of collagen. ... Cretinism is a congenital form of deficiency of thyroid hormones, retarding mental and physical growth. ... This article needs to be cleaned up to conform to a higher standard of quality. ... 5p- karyotype Cri du chat syndrome, also called deletion 5p syndrome, or 5p minus, is a rare genetic disorder due to a missing portion of chromosome 5. ... Diagram of the Human Intestine Crohns disease is a chronic inflammatory disease of the digestive tract and it can involve any part of it - from the mouth to the anus. ...

Cry

• Cryoglobulinemia
• Cryophobia
• Cryptococcosis
• Cryptogenic organized pneumopathy
• Cryptomicrotia brachydactyly syndrome excess fingers
• Cryptomicrotia brachydactyly syndrome
• Cryptophthalmos-syndactyly syndrome
• Cryptorchidism arachnodactyly mental retardation
• Cryroglobulinemia
• Crystal deposit disease
• Crystallophobia

Cryoglobulinemia is the presence of abnormal proteins in the bloodstream which thicken or gel on exposure to cold. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ...

Cu

Cul-Cus

• Culler Jones syndrome
• Curly hair ankyloblepharon nail dysplasia syndrome
• Currarino triad
• Curry Hall syndrome
• Curth-Macklin type ichthyosis hystrix
• Curtis Rogers Stevenson syndrome
• Cushing syndrome, familial
• Cushing's symphalangism
• Cushing's syndrome

Cut

• Cutaneous anthrax
• Cutaneous larva migrans
• Cutaneous lupus erythematosus
• Cutaneous photosensitivity colitis lethal
• Cutaneous T-cell lymphoma
• Cutaneous vascularitis
• Cutis Gyrata syndrome of Beare and Stevenson
• Cutis gyratum acanthosis nigricans craniosynostosis
• Cutis laxa, recessive
• Cutis laxa corneal clouding mental retardation
• Cutis laxa osteoporosis
• Cutis laxa with joint laxity and retarded development
• Cutis laxa, dominant type
• Cutis laxa, recessive type 1
• Cutis laxa, recessive type 2
• Cutis laxa
• Cutis marmorata telangiectatica congenita
• Cutis verticis gyrata mental deficiency
• Cutis verticis gyrata thyroid aplasia mental retardation
• Cutis verticis gyrata
• Cutler Bass Romshe syndrome

Cutaneous larva migrans is a skin disease in humans are caused by a parasitic larvae called Ancylostoma braziliense. ... Cutis verticis gyrata is a superficial condition usually associated with the scalp with sufferers showing some sort of visible folds, ridges or creases on the surface of the scalp. ...

Cy-Cz

• Cyclic neutropenia
• Cyclic vomiting syndrome
• Cyclosporosis
• Cypress facial neuromusculoskeletal syndrome
• Cystathionine beta synthetase deficiency
• Cystic adenomatoid malformation of lung
• Cystic angiomatosis of bone, diffuse
• Cystic fibrosis gastritis megaloblastic anemia
• Cystic fibrosis
• Cystic hamartoma of lung and kidney
• Cystic hygroma lethal cleft palate
• Cystic hygroma
• Cystic medial necrosis of aorta
• Cystin transport, protein defect of
• Cystinosis
• Cystinuria
• Cystinuria-lysinuria
• Cytochrome C oxidase deficiency
• Cytomegalic inclusion disease
• Cytomegalovirus
• Cytoplasmic body myopathy
• Czeizel Losonci syndrome
• Czeizel syndrome