Disease Index
9,486 diseasesmosaic trisomy 4
mosaic trisomy 5
mosaic trisomy 7
MeSH: C537822
mosaic trisomy 8
MeSH: C537940
mosaic trisomy 9
MeSH: C535454
mosaic variegated aneuploidy syndrome 1
Human disease
MeSH: C536987
motor developmental delay due to 14q32.2 paternally expressed gene defect
cause of obesity that results from inheritance of two copies of chromosome 14 from the mother, and no copy of chromosome 14 from the father
motor neuron disease
group of neurological disorders affecting motor neurons
MeSH: D016472
motor stereotypies
human disease
Mouth and genital ulcers with inflamed cartilage syndrome
human disease
movement disorders
clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements
ICD: R25MeSH: D009069
Mowat-Wilson syndrome
rare genetic disorder
MeSH: C536990
Mowat-Wilson syndrome due to a ZEB2 point mutation
human disease
Mowat-Wilson syndrome due to monosomy 2q22
human disease
moya moya disease
cerebral arterial disease characterized by constriction of certain arteries at the base of the brain; blood flow is blocked by the constriction and also by blood clots
MeSH: D009072
Moyamoya syndrome
human disease
Moynahan syndrome
human disease
MeSH: C537052
Moyomoya angiopathy
isolated Moyomoya disease and related syndromes
MPI-CDG
medical condition
MRCS syndrome
human disease
MSA Leben
nonprofit patient organization for Multiple System Atrophy in Germany with services in the German-speaking DACH region.
MSH3-related attenuated familial adenomatous polyposis
human disease
mu chain disease
heavy chain disease that results from an overproduction of mu antibody (IgM)
mucinous adenocarcinoma of the appendix
mucinous tubular and spindle cell carcinoma
human disease
Muckle-Wells syndrome
Human disease
ICD: E85.0
mucolipidosis
human disease
ICD: E77.0MeSH: D009081
mucolipidosis type III
human disease
mucolipidosis type III gamma
human disease
MeSH: C565367
mucolipidosis type IV
Lysosomal storage disease
ICD: E75.1