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List of diseases (M)



A list of diseases in the English wikipedia.

Diseases
Alphabetical list: 0-9 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
See also: Health  |  Exercise  |  Nutrition



Additional recommended knowledge

Contents

Ma

Mac

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

Mad-Mag

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

Mal

  • Mal de debarquement

Mala-Mall

Malo-Malp

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

Man

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

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
  • Mastocytosis, short stature, hearing loss
  • Mastocytosis
  • Mastoiditis
  • 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

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

Me

Mea-Med

Meg-Mei

  • Megacystis microcolon intestinal hypoperistalsis syndrome
  • Megaduodenum
  • Mega-epiphyseal 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

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
  • Membranoproliferative glomerulonephritis (type II)

Men

Mend-Meno

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

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

Met

Meta

  • Metabolic acidosis
  • 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
  • Metatrophic dysplasia
  • Metatropic dwarfism

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

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
  • 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

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

Mis-Mix

Ml-Mn

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

Mo

Mob-Mom

Mon-Moo

Mor-Moy

Mp-Mt

Mu

Muc-Mue

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

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 s-Multiple v

  • 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

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

My

Mya-Myc

Mye-Myi

  • 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
  • Myiasis

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

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, centronuclear
  • Myopathy, desmin storage
  • Myopathy, McArdle type
  • Myopathy, myotubular
  • Myopathy, X-linked, with excessive autophagy
  • Myopathy
  • Myophosphorylase deficiency
  • Myopia
  • Myopia, infantile severe
  • Myopia, severe
  • Myotubular myopathy

Myos-Myot

Myx

  • Myxedema
  • Myxoid liposarcoma
  • Myxoma-spotty pigmentation-endocrine overactivity
  • Myxomatous peritonitis
  • Myxozoa
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "List_of_diseases_(M)". A list of authors is available in Wikipedia.
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