List of diseases (M)

This is a list of diseases starting with the letter "M".

Ma

Mac
  • Mac Dermot Patton Williams syndrome
  • Mac Dermot Winter syndrome

Maci–Macr

Macu

Mad–Mak

Mal

Mala–Mall

Malo–Malp

Man

Mara–Marg

Mari–Mart
  • Marie type ataxia
  • Marie–Unna congenital hypotrichosis
  • Marinesco–Sjögren like syndrome
  • Marinesco–Sjögren 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

Mc

Me

Mea–Med

Meg–Mei

Mel–Mem

Mend–Meno
Mental

Mental d – Mental m

  • Mental deficiency-epilepsy-endocrine disorders
  • Mental mixed retardation deafness 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-polydactyly-uncombable hair

Mer–Mes
  • Mercury poisoning (Mercurialism)
  • 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

Meta

Meth

Mev–Mey

Mi

Mib
  • Mibies syndrome

Mich–Mick
Mircre
  • Micrencephaly corpus callosum agenesis
  • Micrencephaly olivopontocerebellar hypoplasia
Micro
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 q­riplegia
  • Microcephaly, holoprosencephaly, and intrauterine growth retardation
  • Microcephaly, primary autosomal recessive

Microco

Microd – Microv

Micu

Mid–Mir

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

Muli–Mull
Multic–Multin
Multip

Multiple a – Multiple p

Multiple s – Multiple v

Mum–Mut
  • Mumps
  • Münchausen syndrome
  • Münchausen syndrome by proxy
  • 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

Myoa–Myon

Myop

Myos–Myot

Myx
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