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. ...

Ma

Mac

• Mac Ardle disease
• Mac Dermot Patton Williams syndrome
• Mac Dermot Winter syndrome

Maci-Macr

• Macias Flores Garcia Cruz Rivera syndrome
• Mackay Shek Carr syndrome
• Macleod Fraser syndrome
• Macrocephaly cutis marmorata telangiectatica
• Macrocephaly dominant type
• Macrocephaly mental retardation facial dysmorphism
• Macrocephaly mesodermal hamartoma spectrum
• Macrocephaly mesomelic arms talipes
• Macrocephaly pigmentation large hands feet
• Macrocephaly short stature paraplegia
• Macrodactyly of the foot
• Macrodactyly of the hand
• Macroepiphyseal dysplasia Mcalister Coe type
• Macroglobulinemia
• Macroglossia dominant
• Macroglossia exomphalos gigantism
• Macrogyria pseudobulbar palsy
• Macrophagic myofasciitis
• Macrosomia developmental delay dysmorphism
• Macrosomia microphthalmia cleft palate
• Macrothrombocytopenia progressive deafness
• Macrothrombocytopenia with leukocyte inclusions

Macu

• Macular corneal dystrophy
• Macular degeneration juvenile
• Macular degeneration, age-related
• Macular degeneration, polymorphic
• Macular degeneration
• Macular dystrophy, vitelliform
• Macules hereditary congenital hypopigmented and hyperpigmented

This article or section should be merged with age-related macular degeneration Macular degeneration is a medical condition where the light sensing cells in the macula malfunction and over time cease to work. ...

Mad-Mag

• Mad cow disease
• Madelung's disease
• Madokoro Ohdo Sonoda syndrome
• Maffucci syndrome
• Mageirocophobia
• Maghazaji syndrome
• Magnesium defect in renal tubular transport of
• Magnesium wasting renal

Bovine spongiform encephalopathy (BSE or commonly mad cow disease) is a fatal, neurodegenerative disease of cattle, which infects by a mechanism that shocked biologists on its discovery in late 20th century and appears transmissible to humans. ... Maghazaji syndrome is a human genetic disorder that is characterised as the combination of two congenital disorders hemifacical microsomia and partial gigantism. ...

Mal

• Mal de debarquement

Mal de debarquement Syndrome (MDD or MDDS) is a quite rare disease. ...

Mala-Mall

• Malakoplakia
• Malaria
• Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency
• Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency
• Male pseudohermaphroditism due to defective LH molecule
• Malformations in neuronal migration
• Malignant astrocytoma
• Malignant fibrous histiocytoma
• Malignant germ cell tumor
• Malignant hyperthermia arthrogryposis torticollis
• Malignant hyperthermia susceptibility type 1
• Malignant hyperthermia susceptibility type 2
• Malignant hyperthermia susceptibility type 3
• Malignant hyperthermia susceptibility type 4
• Malignant hyperthermia susceptibility type 5
• Malignant hyperthermia susceptibility type 6
• Malignant hyperthermia
• Malignant mesenchymal tumor
• Malignant mixed Mullerian tumor
• Malignant paroxysmal ventricular tachycardia
• Mallory-Weiss syndrome

Red blood cell infected with Malaria (Italian: bad air; formerly called ague or marsh fever in English) is an infectious disease which in humans causes about 500 million infections and 2 million deaths annually, mainly in the tropics and sub-Saharan Africa. ... Malignant hyperthermia is a life-threatening condition resulting from a genetic sensitivity of skeletal muscles to volatile anaesthetics and depolarizing neuromuscular blocking drugs that occurs during or after anaesthesia. ... Mallory-Weiss Syndrome refers to bleeding from tears in the mucosa at the junction of the stomach and esophagus, usually caused by severe retching, coughing, or vomiting. ...

Malo-Malp

• Malonic aciduria
• Malonyl-CoA decarboxylase deficiency
• Malouf syndrome
• Malpuech facial clefting syndrome

Malouf syndrome (also known as congestive cardiomyopathy-hypergonadotropic hypogonadism syndrome) is a congenital disorder that causes one or more of the following symptoms: Mental retardation, ovarian dysgenesis, congestive cardiomyopathy, broad nasal base, blepharoptosis, and bone abnormalities, and occasionally marfanoid habitus (tall stature with long and thin limbs, little subcutaneous fat...

Man

• Mandibuloacral dysplasia
• Mandibulofacial dysostosis deafness postaxial polydactly
• Manic Depression, Bipolar
• Manic-depressive psychosis, genetic types
• Mannosidosis
• Manouvrier syndrome
• Mansonelliasis
• Mantle cell lymphoma

Mar

Mara-Marg

• Marashi Gorlin syndrome
• Marburg fever
• Marchiafava Bignami disease
• Marchiafava-Micheli disease
• Marcus Gunn phenomenon
• Marden Walker like syndrome
• Marden-Walker syndrome
• Marek disease
• Marfan Syndrome type II
• Marfan Syndrome type III
• Marfan Syndrome type IV
• Marfan Syndrome type V
• Marfan syndrome
• Marfan-like syndrome, Boileau type
• Marfan-Like syndrome
• Marfanoid craniosynostosis syndrome
• Marfanoid hypermobility
• Marfanoid mental retardation syndrome autosomal
• Marginal glioneuronal heterotopia

The Marburg virus is the causative agent of Marburg hemorrhagic fever. ... Marfan syndrome is a connective tissue disorder, affecting many structures, including the skeleton, lungs, eyes, heart and blood vessels. ...

Mari-Mart

• Marie type ataxia
• Marie Unna congenital hypotrichosis
• Marinesco Sjogren like syndrome
• Marinesco-Sjogren syndrome
• Marion Mayers syndrome
• Markel Vikkula Mulliken syndrome
• Marles Greenberg Persaud syndrome
• Maroteaux Cohen Solal Bonaventure syndrome
• Maroteaux Fonfria syndrome
• Maroteaux Le Merrer Bensahel syndrome
• Maroteaux Stanescu Cousin syndrome
• Maroteaux Verloes Stanescu syndrome
• Maroteaux-Lamy syndrome
• Marphanoid syndrome type De Silva
• Marsden Nyhan Sakati syndrome
• Marsden syndrome
• Marshall syndrome
• Marshall-Smith syndrome
• Martinez Monasterio Pinheiro syndrome
• Martsolf Reed Hunter syndrome
• Martsolf syndrome

Mas-May

• MASA syndrome
• Mass syndrome
• Massa Casaer Ceulemans syndrome
• Mast cell disease
• Mastigophobia
• Mastocytosis, short stature, hearing loss
• Mastocytosis
• Mastroiacovo De Rosa Satta syndrome
• Mastroiacovo Gambi Segni syndrome
• MAT deficiency
• Maternal hyperphenylalaninemia
• Maternally inherited diabetes and deafness
• Mathieu De Broca Bony syndrome
• Matsoukas Liarikos Giannika syndrome
• Matthew-Wood syndrome
• Maturity onset diabetes of the young
• Maumenee syndrome
• Maxillary double lip
• Maxillofacial dysostosis
• Maxillonasal dysplasia, Binder type
• Mayer Rokitanski Kuster syndrome
• May-Hegglin Anomaly

MASA syndrome is a rare hereditary neurological disorder. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... In medicine, mastocytosis is a group of rare disorders of both children and adults caused by the presence of too many mast cells (mastocytes) in a persons body. ... Maturity onset diabetes of the young (MODY) refers to any of several rare hereditary forms of diabetes mellitus due to dominantly inherited defects of insulin secretion. ...

Mc

• McAlister Crane syndrome
• McArdle disease
• McCallum Macadam Johnston syndrome
• McCune-Albright syndrome
• McDonough syndrome
• McDowall syndrome
• McGillivray syndrome
• McKusick Kaufman syndrome
• McKusick type metaphyseal chondrodysplasia
• McLain Debakian syndrome
• McPherson Clemens syndrome
• McPherson Robertson Cammarano syndrome

McArdle disease (sometimes called McArdles disease or muscle phosphorylase deficiency) is a metabolic disorder, more specifically a glycogen storage disease, caused by a deficiency of the enzyme muscle phosphorylase (sometimes known as myophosphorylase). ...

Me

Mea-Med

• Meacham Winn Culler syndrome
• Meadows syndrome
• Measles
• Meckel like syndrome
• Meckel syndrome
• Medeira Dennis Donnai syndrome
• Median cleft lip corpus callosum lipoma skin polyps
• Median nodule of the upper lip
• Mediastinal endodermal sinus tumors
• Mediterranean fever
• Medium-chain Acyl-CoA dehydrogenase deficiency
• Medrano Roldan syndrome
• Medullary cystic disease
• Medullary thyroid carcinoma
• Medulloblastoma

Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder that affects groups of patients originating from around the Mediterranean Sea (hence its name). ...

Meg-Mei

• Megacystis microcolon intestinal hypoperistalsis syndrome
• Megaduodenum
• Megaepiphyseal dwarfism
• Megalencephalic leukodystrophy
• Megalencephaly-cystic leukodystrophy
• Megaloblastic anemia
• Megalocornea mental retardation syndrome
• Megalocytic Interstitial Nephritis
• Mehes syndrome
• Mehta Lewis Patton syndrome
• Meier Blumberg Imahorn syndrome
• Meier Rotschild syndrome
• Meige syndrome
• Meigel disease
• Meinecke Pepper syndrome
• Meinecke syndrome

Megaloblastic anemia is anemia resulting from a deficiency of vitamin B12 and folic acid. ...

Mel-Mem

• Melanoma type 1
• Melanoma type 2
• Melanoma, familial
• Melanoma, Malignant
• Melanoma-astrocytoma syndrome
• Melanosis neurocutaneous
• MELAS
• Meleda Disease
• Melhem Fahl syndrome
• Melioidosis
• Melkersson-Rosenthal syndrome
• Melnick-Needles osteodysplasty
• Melnick-Needles syndrome
• Melophobia
• Membranoproliferative glomerulonephritis (type II)

Melioidosis, also known as pseudoglanders and Whitmores disease (after Capt Alfred Whitmore) is an uncommon infectious disease caused by a Gram-negative bacterium, Burkholderia pseudomallei, found in soil and water. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ...

Men

Mend-Meno

• Mendelian susceptibility to atypical mycobacteria
• Menetrier's disease
• Mengel Konigsmark syndrome
• Ménière's disease
• Meningeal angiomatosis cleft hypoplastic left heart
• Meningioma 1
• Meningioma
• Meningitis, meningococcal
• Meningitis
• Meningocele
• Meningococcemia
• Meningoencephalocele
• Meningoencephalocele-arthrogryposis-hypoplastic thumb
• Meningomyelocele
• Menophobia

Ménière’s disease (or syndrome, since its cause is unknown) was first described by French physician Prosper Ménière in 1861. ... Meningiomas are tumors arising from the outer part of the arachnoid mater in the meninges of the brain or the spinal cord. ... Meningitis is inflammation of the membranes (meninges) covering the brain and the spinal cord. ...

Ment

Menta

Mental

Mental d-Mental m

• Mental deficiency-epilepsy-endocrine disorders
• Mental mixed retardation deafnes clubbed digits

Mental r Mental retardation a-Mental retardation m

• Mental retardation anophthalmia craniosynostosis
• Mental retardation arachnodactyly hypotonia telangiectasia
• Mental retardation athetosis microphthalmia
• Mental retardation blepharophimosis obesity web neck
• Mental retardation Buenos Aires type
• Mental retardation cataracts calcified pinnae myopathy
• Mental retardation coloboma slimness
• Mental retardation contractural arachnodactyly
• Mental retardation dysmorphism hypogonadism diabetes
• Mental retardation epilepsy bulbous nose
• Mental retardation epilepsy
• Mental retardation gynecomastia obesity X linked
• Mental retardation hip luxation G6PD variant
• Mental retardation hypocupremia hypobetalipoproteinemia
• Mental retardation hypotonia skin hyperpigmentation
• Mental retardation macrocephaly coarse facies hypotonia
• Mental retardation microcephaly phalangeal facial
• Mental retardation microcephaly unusual facies
• Mental retardation Mietens Weber type
• Mental retardation multiple nevi
• Mental retardation myopathy short stature endocrine defect
• Mental retardation nasal hypoplasia obesity genital hypoplasia

Mental retardation n-Mental retardation s

• Mental retardation nasal papillomata
• Mental retardation osteosclerosis
• Mental retardation progressive spasticity
• Mental retardation psychosis macroorchidism
• Mental retardation short broad thumbs
• Mental retardation short stature absent phalanges
• Mental retardation short stature Bombay phenotype
• Mental retardation short stature cleft palate unusual facies
• Mental retardation short stature deafness genital
• Mental retardation short stature hand contractures genital anomalies
• Mental retardation short stature heart and skeletal anomalies
• Mental retardation short stature hypertelorism
• Mental retardation short stature microcephaly eye
• Mental retardation short stature ocular and articular anomalies
• Mental retardation short stature scoliosis
• Mental retardation short stature unusual facies
• Mental retardation short stature wedge shaped epiphyses
• Mental retardation skeletal dysplasia abducens palsy
• Mental retardation Smith Fineman Myers type
• Mental retardation spasticity ectrodactyly

Mental retardation u-Mental retardation x

• Mental retardation unusual facies Ampola type
• Mental retardation unusual facies Davis Lafer type
• Mental retardation unusual facies talipes hand anomalies
• Mental retardation unusual facies
• Mental retardation Wolff type
• Mental retardation X linked Atkin type
• Mental retardation X linked borderline Maoa metabolism anomaly
• Mental retardation X linked Brunner type
• Mental retardation X linked dysmorphism
• Mental retardation X linked dystonia dysarthria
• Mental retardation X linked severe Gustavson type
• Mental retardation X linked short stature obesity
• Mental retardation X linked Tranebjaerg type seizures psoriasis
• Mental retardation, unexplained
• Mental retardation, X linked, Marfanoid habitus
• Mental retardation, X linked, nonspecific
• Mental retardation, X-linked 14
• Mental retardation
• Mental retardation-polydactyly-uncombable hair

Mental retardation (also called mental handicap and the UK Mental Health Act (1983) defines mental impairment and severe mental impairment) is a term for a pattern of persistently slow learning of basic motor and language skills (milestones) during childhood, and a significantly below-normal intellectual capacity as an adult. ...

Mer-Mes

• Mercury poisoning
• Meretoja syndrome
• Merkle tumors
• Merlob Grunebaum Reisner syndrome
• Merlob syndrome
• Mesangial sclerosis, diffuse
• Mesenteric ischemia
• Mesenteric panniculitis
• Mesodermal defects lower type
• Mesomelia synostoses
• Mesomelia
• Mesomelic dwarfism cleft palate camptodactyly
• Mesomelic dwarfism Langer type
• Mesomelic dwarfism Nievergelt type
• Mesomelic dwarfism Reinhardt Pfeiffer type
• Mesomelic dysplasia skin dimples
• Mesomelic dysplasia Thai type
• Mesomelic syndrome Pfeiffer type
• Mesothelioma

General Name, Symbol, Number Mercury, Hg, 80 Chemical series transition metals Group, Period, Block 12 (IIB), 6, d Density, Hardness liquid 13. ...

Met

Meta

• Metabolic disorder
• Metabolic Syndrome X
• Metacarpals 4 and 5 fusion
• Metachondromatosis
• Metageria
• Metaphyseal anadysplasia
• Metaphyseal chondrodysplasia Schmid type
• Metaphyseal chondrodysplasia Spahr type
• Metaphyseal chondrodysplasia, others
• Metaphyseal dysostosis mental retardation conductive deafness
• Metaphyseal dysplasia maxillary hypoplasia brachydactyly
• Metaphyseal dysplasia Pyle type
• Metastatic insulinoma
• Metatarsus adductus
• Metathesiophobia
• Metatrophic dysplasia
• Metatropic dwarfism

Metathesiophobia is the fear of changes. ...

Meth

• Methimazole antenatal infection
• Methionine adenosyl transferase deficiency
• Methyl mercury antenatal infection
• Methylcobalamin deficiency cbl G type
• Methylcobalamin deficiency, cbl E complementation type
• Methylenetetrahydrofolate reductase deficiency
• Methylmalonic acidemia with homocystinuria
• Methylmalonic acidemia
• Methylmalonic aciduria microcephaly cataract
• Methylmalonicacidemia with homocystinuria, cbl D
• Methylmalonicaciduria with homocystinuria, cbl F
• Methylmalonicaciduria, vitamin B12 unresponsive, mut-0
• Methylmalonyl-Coenzyme A mutase deficiency

Methylmalonic acidemia is an inborn error of intermediary metabolism that may present in the early neonatal period with progressive encephalopathy and death due to a secondary hyperammonemia. ...

Mev-Mey

• Mevalonate kinase deficiency
• Mevalonicaciduria
• Meyenburg-Altherr-Uehlinger syndrome

Mi

Mic

Mich-Mick

• Michelin tire baby syndrome
• Michels Caskey syndrome
• Michels syndrome
• Mickleson syndrome

Micr

Mircre

• Micrencephaly corpus callosum agenesis
• Micrencephaly olivopontocerebellar hypoplasia

Micro

• Micro syndrome

Microb

• Microbrachycephaly ptosis cleft lip

Microc

Microcephalic

• Microcephalic osteodysplastic primordial dwarfism
• Microcephalic primordial dwarfism Toriello type
• Microcephalic primordial dwarfism

Microcephaly Microcephaly a-Microcephaly l

• Microcephaly albinism digital anomalies syndrome
• Microcephaly autosomal dominant
• Microcephaly brachydactyly kyphoscoliosis
• Microcephaly brain defect spasticity hypernatremia
• Microcephaly cardiac defect lung malsegmentation
• Microcephaly cardiomyopathy
• Microcephaly cervical spine fusion anomalies
• Microcephaly chorioretinopathy recessive form
• Microcephaly cleft palate autosomal dominant
• Microcephaly deafness syndrome
• Microcephaly developmental delay pancytopenia
• Microcephaly facial clefting preaxial polydactyly
• Microcephaly glomerulonephritis Marfanoid habitus
• Microcephaly hiatus hernia nephrotic syndrome
• Microcephaly hypergonadotropic hypogonadism short stature
• Microcephaly immunodeficiency lymphoreticuloma
• Microcephaly intracranial calcification
• Microcephaly lymphoedema chorioretinal dysplasia
• Microcephaly lymphoedema syndrome

Microcephaly m-Microcephaly w

• Microcephaly mental retardation retinopathy
• Microcephaly mental retardation spasticity epilepsy
• Microcephaly mesobrachyphalangy tracheoesophageal fistula syndrome
• Microcephaly microcornea syndrome Seemanova type
• Microcephaly micropenis convulsions
• Microcephaly microphthalmos blindness
• Microcephaly nonsyndromal
• Microcephaly pontocerebellar hypoplasia dyskinesia
• Microcephaly seizures mental retardation heart disorders
• Microcephaly sparse hair mental retardation seizures
• Microcephaly syndactyly brachymesophalangy
• Microcephaly with chorioretinopathy, autosomal dominant form
• Microcephaly with normal intelligence, immunodeficiency
• Microcephaly with spastic quadriplegia
• Microcephaly, holoprosencephaly, and intrauterine growth retardation
• Microcephaly, primary autosomal recessive
• Microcephaly

Microco

• Microcoria, congenital
• Microcornea corectopia macular hypoplasia
• Microcornea glaucoma absent frontal sinuses

Microd-Microv

• Microdontia hypodontia short stature
• Microencephaly
• Microgastria limb reduction defect
• Microgastria short stature diabetes
• Microinfarct
• Micromelic dwarfism Fryns type
• Micromelic dysplasia dislocation of radius
• Microphobia
• Microphtalmos bilateral colobomatous orbital cyst
• Microphthalmia camptodactyly mental retardation
• Microphthalmia cataract
• Microphthalmia diaphragmatic hernia Fallot
• Microphthalmia mental deficiency
• Microphthalmia microtia fetal akinesia
• Microphthalmia, Lentz type
• Microphthalmia
• Microphthalmos, microcornea, and sclerocornea
• Microscopic polyangiitis
• Microsomia hemifacial radial defects
• Microspherophakia metaphyseal dysplasia
• Microsporidiosis
• Microtia, meatal atresia and conductive deafness
• Microvillus inclusion disease

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

Micu

• Miculicz syndrome

Mid-Mir

• MIDAS syndrome
• Midline cleft of lower lip
• Midline defects autosomal type
• Midline defects recessive type
• Midline developmental field defects
• Midline field defects
• Midline lethal granuloma
• Mietens syndrome
• Mievis Verellen Dumoulin syndrome
• Migraine
• Mikulicz' Disease
• Mikulicz syndrome
• Miller Fisher syndrome
• Miller-Dieker syndrome
• Milner Khallouf Gibson syndrome
• MILS syndrome
• Minkowski-Chauffard disease
• Minoxidil antenatal infection
• Miosis, congenital
• Mirror hands feet nasal defects
• Mirror polydactyly segmentation and limbs defects

Miller-Dieker Syndrome is a disease characterised by a developmental defect of the brain, caused by incomplete neuronal migration. ...

Mis-Mix

• Misophobia
• Mitochondrial cytopathy (generic term)
• Mitochondrial diseases of nuclear origin
• Mitochondrial diseases, clinically undefinite
• Mitochondrial Diseases
• Mitochondrial encephalomyopathy aminoacidopathy
• Mitochondrial genetic disorders
• Mitochondrial myopathy lactic acidosis
• Mitochondrial myopathy-encephalopathy-lactic acidosis
• Mitochondrial PEPCK deficiency
• Mitochondrial trifunctional protein deficiency
• Mitral atresia
• Mitral regurgitation deafness skeletal anomalies
• Mitral valve prolapse, familial, autosomal dominant
• Mitral valve prolapse, familial, X linked
• Mitral valve prolapse
• Miura syndrome
• Mixed connective tissue disease
• Mixed Mullerian tumor
• Mixed sclerosing bone dystrophy

Mitochondrial diseases are a group of disorders relating to the mitochondria, the organelles that are the powerhouses of the eukaryotic cells that comprise higher-order lifeforms (including humans). ... Mitral valve prolapse (MVP) is a heart valve condition marked by the displacement of an abnormally thickened mitral valve leaflet into the left atrium during systole. ...

Ml-Mn

• MLS syndrome
• MMEP syndrome
• MMT syndrome
• MN1
• MNGIE syndrome

Mo

Mob-Mom

• Mobius syndrome
• MODY syndrome
• Moebius axonal neuropathy hypogonadism
• Moebius syndrome
• Moerman Van den berghe Fryns syndrome
• Moeschler Clarren syndrome
• Mohr syndrome
• Mohr-Tranebjaerg syndrome
• Mollica Pavone Antener syndrome
• Molluscum contagiosum
• Moloney syndrome
• Molybdenum cofactor deficiency
• MOMO syndrome

Clinical features Mobius syndrome(Moebius is an alternate spelling, the two can be used interchangeably)is caused by an abnormal neurodevelopment of the cranial nerves. ... Maturity onset diabetes of the young (MODY) refers to any of several rare hereditary forms of diabetes mellitus due to dominantly inherited defects of insulin secretion. ... Clinical features Mobius syndrome(Moebius is an alternate spelling, the two can be used interchangeably)is caused by an abnormal neurodevelopment of the cranial nerves. ... Molluscum contagiosum (also called water wart) is skin disease caused by the molluscum contagiosum virus (or MCV), a DNA poxvirus. ... MOMO syndome is a very rare genetic disorder which has been diagnosed in only four cases around the world. ...

Mon-Moo

• Mondini Dysplasia
• Mondor's disease
• Monilethrix
• Monoamine oxidase A deficiency
• Monoclonal gammopathy of undetermined significance
• Monodactyly tetramelic
• Mononen Karnes Senac syndrome
• Mononeuritis multiplex
• Monosomy 8q12 21
• Monosomy 8q21 q22
• Monosomy X
• Montefiore syndrome
• Moore Federman syndrome
• Moore Smith Weaver syndrome

Mondini Dysplasia Mondini dysplasia (sometimes known as a Mondini malformation) is a cause of hearing loss. ... Mondors disease is a rare condition which involves thrombophlebitis of the superficial veins of the breast and anterior chest wall. ...

Mor-Moy

• Morel's ear
• Moreno Zachai Kaufman syndrome
• Morgani Turner Albright syndrome
• Morhosseini Holmes Walton syndrome
• Morillo Cucci Passarge syndrome
• Morphea Scleroderma
• Morphea, generalized
• Morquio disease, type A
• Morquio disease, type B
• Morquio syndrome
• Morrison Young syndrome
• Morse Rawnsley Sargent syndrome
• Motor neuron disease
• Motor neuro-ophthalmic disorders
• Motor neuropathy peripheral dysautonomia
• Motor neuropathy
• Motor sensory neuropathy type 1 aplasia cutis congenita
• Motorphobia
• Mounier-Kuhn syndrome
• Mount Reback syndrome
• Mousa Al din Al Nassar syndrome
• Moyamoya disease

Motor Neurone Disease (MND) is a term used to cover a number of illnesses of the motor neurone. ...

Mp-Mt

• MPO deficiency
• MPS III-A
• MPS III-B
• MPS III-C
• MPS III-D
• MPS VI
• MR
• MRKH Syndrome
• MSBD syndrome
• MTHFR deficiency

Myeloperoxidase deficiency is a genetic disorder featuring deficiency of myeloperoxidase. ... In ordinary English, Mr is a written abbreviation for Mister. MR can also stand for: Magnetic resonance imaging, properly abbreviated MRI Magyar Rádió, a Hungarian radio station Master of the Rolls, the presiding officer of the Civil Division of the Court of Appeal in the UK legal system Mathematical Reviews...

Mu

Muc-Mue

• Mucha-Habermann disease
• Muckle-Wells syndrome
• Mucoepithelial dysplasia
• Mucolipidosis type 1
• Mucolipidosis type 3
• Mucolipidosis type 4
• Mucopolysaccharidosis type 3
• Mucopolysaccharidosis type 4
• Mucopolysaccharidosis type I Hurler syndrome
• Mucopolysaccharidosis type I Hurler/Scheie syndrome
• Mucopolysaccharidosis type I Scheie syndrome
• Mucopolysaccharidosis type II Hunter syndrome- mild form
• Mucopolysaccharidosis type II Hunter syndrome- severe form
• Mucopolysaccharidosis type IV-A Morquio syndrome
• Mucopolysaccharidosis type IV-B
• Mucopolysaccharidosis type V
• Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate
• Mucopolysaccharidosis type VII Sly syndrome
• Mucopolysaccharidosis
• Mucosulfatidosis
• Muenke Syndrome

Mucolpolysaccharidosis Type VII or Sly syndrome (named after its discoverer William Sly in 1969) is also sometimes called MPS. The defective gene lies on chromosome 7. ... The mucopolysaccharidoses are inborn errors of metabolism resulting from the deficiency of specific lysosomal enzymes needed in glycosaminoglycan catabolism. ...

Mul

Muli-Mull

• Mulibrey Nanism syndrome
• Muller Barth Menger syndrome
• Mullerian agenesis
• Mullerian aplasia
• Mullerian derivatives lymphangiectasia polydactyly
• Mullerian derivatives, persistent
• Mullerian duct abnormalities galactosemia
• Mulliez Roux Loterman syndrome

Mullerian agenesis refers to a condition in a female where the mullerian ducts fail to develop and a uterus will not be present. ...

Mult

Multi

Multic-Multin

• Multicentric osteolysis nephropathy
• Multicentric reticulohistiocytosis
• Multifocal heterotopia
• Multifocal motor neuropathy with conduction block
• Multifocal ventricular premature beats
• Multinodular goiter cystic kidney polydactyly

Multip

Multiple a-Multiple p

• Multiple acyl-CoA deficiency
• Multiple carboxylase deficiency, biotin responsive
• Multiple carboxylase deficiency, late onset
• Multiple carboxylase deficiency, propionic acidemia
• Multiple chemical sensitivity
• Multiple congenital anomalies mental retardation, growth failure and cleft lip palate
• Multiple congenital contractures
• Multiple contracture syndrome Finnish type
• Multiple endocrine neoplasia type 1
• Multiple endocrine neoplasia, type 2
• Multiple fibrofolliculoma familial
• Multiple hereditary exostoses
• Multiple joint dislocations metaphyseal dysplasia
• Multiple myeloma
• Multiple organ failure
• Multiple pterygium syndrome lethal type
• Multiple pterygium syndrome

Multiple s-Multiple v Multiple chemical sensitivity (MCS), also known as 20th Century Syndrome, Environmental illness, Sick Building Syndrome, Idiopathic Environmental Intolerance (IEI), can be defined as a chronic, recurring disease caused by a persons inability to tolerate an environmental chemical or class of foreign chemicals according to the NIH National Institute of... Multiple myeloma (also known simply as myeloma or plasma cell myeloma) is a presently incurable hematological malignancy of plasma cells, the cells of the immune system that produce antibodies. ... Multiple organ dysfunction syndrome - M.O.D.S. (previously known as multiple organ failure) is altered organ function in an acutely ill patient requiring medical intervention to maintain homeostasis. ...

• Multiple sclerosis ichthyosis factor VIII deficiency
• Multiple sclerosis
• Multiple subcutaneous angiolipomas
• Multiple sulfatase deficiency
• Multiple synostoses syndrome 1
• Multiple system atrophy
• Multiple vertebral anomalies unusual facies

Multiple System Atrophy (MSA) is a rare and always terminal degenerative neurological disorder characterized by a combination of Parkinsonism, cerebellar or corticospinal signs, pyramidal signs, and autonomic dysfunction. ...

Mum-Mut

• Mumps
• Munchausen by proxy syndrome
• Muscle-eye-brain syndrome
• Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus
• Muscular dystrophy congenital infantile cataract hypogonadism
• Muscular dystrophy congenital, merosin negative
• Muscular dystrophy facioscapulohumeral
• Muscular dystrophy Hutterite type
• Muscular dystrophy limb girdle type 2A, Erb type
• Muscular dystrophy limb-girdle autosomal dominant
• Muscular dystrophy limb-girdle type 2B, Myoshi type
• Muscular dystrophy limb-girdle with beta-sarcoglycan deficiency
• Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
• Muscular dystrophy white matter spongiosis
• Muscular dystrophy, congenital, merosin-positive
• Muscular dystrophy, Duchenne and Becker type
• Muscular dystrophy
• Muscular fibrosis multifocal obstructed vessels
• Muscular phosphorylase kinase deficiency
• Mutations in estradiol receptor

The muscular dystrophies are a group of genetic and hereditary muscle diseases; characterized by progressive skeletal muscle weakness, defects in muscle proteins, and the death of muscle cells and tissue. ...

My

Mya-Myc

• Myalgia eosinophilia associated with tryptophan
• Myalgic encephalomyelitis
• Myasthenia gravis congenital
• Myasthenia gravis
• Myasthenia, familial
• Mycetoma
• Mycobacterium avium complex infection
• Mycophobia
• Mycoplasmal pneumonia
• Mycosis fungoides lymphoma
• Mycosis fungoides, familial
• Mycosis fungoides
• Mycositis fungoides

Chronic fatigue syndrome (CFS) is a condition of excessive fatigue, cognitive impairment and other varied symptoms. ... Myasthenia gravis or MG is a disease in which antibodies destroy neural receptor cells in muscle tissue. ... The English suffix -phobia is used to describe fear or hatred (the latter is often ignored) of a particular thing or subject. ... Mycosis Fungoides, also known as Alibert-Bazin syndrome or granuloma fungoides, is a rare form of non-Hodgkins lymphoma cancer. ...

Mye-Myh

• Myelinopathies
• Myelitis
• Myelocerebellar disorder
• Myelodysplasia
• Myelodysplastic syndromes
• Myelofibrosis, idiopathic
• Myelofibrosis
• Myelofibrosis-osteosclerosis
• Myeloid splenomegaly
• Myeloperoxidase deficiency
• Myhre Ruvalcaba Graham syndrome
• Myhre Ruvalcaba Kelley syndrome
• Myhre School syndrome
• Myhre syndrome

Myelitis is a human disease involving swelling of the spinal cord, which disrupts central nervous system functions linking brain and limbs. ... The myelodysplastic syndromes (MDS, formerly known as preleukemia) are a diverse collection of haematological conditions united by ineffective production of blood cells. ... Myelofibrosis is the gradual replacement of the bone marrow by connective tissue. ... Myeloperoxidase deficiency is a genetic disorder featuring deficiency of myeloperoxidase. ...

Myo

Myoa-Myon

• Myoadenylate deaminase deficiency
• Myocarditis
• Myocardium disorder
• Myoclonic dystonia
• Myoclonic progressive familial epilepsy
• Myoclonus ataxia
• Myoclonus cerebellar ataxia deafness
• Myoclonus epilepsy partial seizure
• Myoclonus epilepsy
• Myoclonus hereditary progressive distal muscular atrophy
• Myoclonus progressive epilepsy of Unverricht and Lundborg
• Myoclonus with epilepsy with ragged red fibers (mitochondria)
• Myoclonus
• Myofibrillar lysis
• Myofibroblastic tumors
• Myoglobinuria dominant form
• Myoglobinuria recurrent
• Myoglobinuria
• Myoneurogastrointestinal encephalopathy syndrome

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). ... In medicine (cardiology), myocarditis is inflammation of the myocardium, the muscular part of the heart. ... Myoclonus is brief, involuntary twitching of a muscle or a group of muscles. ...

Myop

• Myopathy and diabetes mellitus
• Myopathy cataract hypogonadism
• Myopathy congenital multicore with external ophthalmoplegia
• Myopathy growth and mental retardation hypospadias
• Myopathy Hutterite type
• Myopathy mitochondrial cataract
• Myopathy Moebius Robin syndrome
• Myopathy ophthalmoplegia hypoacousia areflexia
• Myopathy tubular aggregates
• Myopathy with lactic acidosis and sideroblastic anemia
• Myopathy with lysis of myofibrils
• Myopathy, desmin storage
• Myopathy, McArdle type
• Myopathy, myotubular
• Myopathy, X-linked, with excessive autophagy
• Myopathy
• Myophosphorylase deficiency
• Myopia
• Myopia, infantile severe
• Myopia, severe

In medicine, a myopathy is a neuromuscular disease in which the muscle fibers dysfunction for any one of many reasons, resulting in muscular weakness. ... Normal vision for a achromatopsic colour-blind person. ...

Myos-Myot

• Myositis ossificans post-traumatic
• Myositis ossificans progressiva
• Myositis ossificans
• Myositis, inclusion body
• Myositis
• Myotonia atrophica
• Myotonia mental retardation skeletal anomalies

Myx

• Myxedema
• Myxoid liposarcoma
• Myxoma-spotty pigmentation-endocrine overactivity
• Myxomatous peritonitis
• Myxozoa