Disease Index
9,486 diseasesmultiple sclerosis-ichthyosis-factor VIII deficiency syndrome
multiple sclerosis, susceptibility to
human disease
multiple sclerosis, susceptibility to, 5
human disease
multiple symmetric lipomatosis
skin condition characterized by extensive symmetric fat deposits in the head, neck, and shoulder girdle area
ICD: E88.8MeSH: D008069
multiple system atrophy
neurodegenerative disorder characterized by autonomic failure, parkinsonism, cerebellar impairment and corticospinal signs, with a median survival of 6-9 years
ICD: G232MeSH: D019578
multiple system atrophy, cerebellar type
Multiple system atrophy, cerebellar type (MSA-c) is a form of multiple system atrophy (MSA; see this term) with predominant cerebellar features (gait and limb ataxia, oculomotor dysfunction, and dysarthria)
multiple system atrophy, parkinsonian type
Multiple system atrophy, parkinsonian type (MSA-p) is a form of multiple system atrophy (MSA; see this term) with predominant parkinsonian features (bradykinesia, rigidity, irregular jerky postural tremor, and postural instability)
multisystemic smooth muscle dysfunction syndrome
medical condition
MURCS association
medical condition
ICD: Q87.8
muscle tissue neoplasm
human disease
MeSH: D009379
muscle-eye-brain disease
disease
muscle-eye-brain disease with bilateral multicystic leucodystrophy
muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
This disorder is characterized by muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
MeSH: C538193
muscular channelopathy
channelopathy that involves the muscle tissue
muscular dystrophy
diseases that weaken the body's muscles
MeSH: D009136
muscular dystrophy-dystroglycanopathy
Human disease
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9
human disease
muscular dystrophy-dystroglycanopathy type B6
human disease
MeSH: C563844
muscular dystrophy-white matter spongiosis syndrome
human disease
muscular fibrosis multifocal obstructed vessels
human disease
muscular glycogenosis
human disease
muscular hypertrophy-hepatomegaly-polyhydramnios syndrome
human disease
muscular lipidosis
human disease
musculoskeletal disease with cataract
human disease
myasthenia gravis
human disease
MeSH: D009157
myasthenic syndrome with eye involvement
human disease
mycetoma
chronic subcutaneous infection caused by aerobic actinomycetic bacteria or fungi
ICD: B47MeSH: D008271
Mycobacterium xenopi infection
disease caused by infection with Mycobacterium xenopi
mycophenolate mofetil embryopathy
Mycophenolate mofetil (MMF) embryopathy is a malformative syndrome due to the teratogenic effect of MMF, an effective immunosuppressive agent widely used for the prevention of organ rejection after organ transplantation
Mycoplasma encephalitis