Disease Index
9,486 diseasesMarshall syndrome
medical condition
ICD: Q87.0MeSH: C536025
Marshall–Smith syndrome
syndrome that is characterized by advanced bone age, failure to thrive, respiratory problems, dysmorphic facial features, and variable mental retardation
MeSH: C536026
Martinez-Frias syndrome
human disease
MeSH: C563346
MASS syndrome
Connective tissue disorder
ICD: Q87.5MeSH: C536030
mast cell leukemia
rare leukemia (blood cancer) involving mast cells
ICD: C94.3MeSH: D007946
mast cell sarcoma
human disease
MeSH: D012515
mast syndrome
hereditary spastic paraplegia associated with dementia
MeSH: C565409
mastocytosis
human disease
MeSH: D008415
maternal 14q32.2 hypermethylation syndrome
human disease
maternal 14q32.2 microdeletion syndrome
human disease
maternal disease-related embryofetopathy
human disease
maternal hyperthermia induced birth defects
maternal phenylketonuria
condition occurring in untreated or partially treated females with phenylketonuria when they become pregnant
MeSH: D017042
maternal riboflavin deficiency
human disease
maternal uniparental disomy of chromosome 1
human disease
maternal uniparental disomy of chromosome 13
human disease
maternal uniparental disomy of chromosome 14
human disease
maternal uniparental disomy of chromosome 16
human disease
maternal uniparental disomy of chromosome 2
human disease
maternal uniparental disomy of chromosome 20
human disease
maternal uniparental disomy of chromosome 21
human disease
maternal uniparental disomy of chromosome 22
human disease
maternal uniparental disomy of chromosome 4
human disease
maternal uniparental disomy of chromosome 6
human disease
maternal uniparental disomy of chromosome 9
human disease
maternal uniparental disomy of chromosome X
human disease
maternally-inherited cardiomyopathy and hearing loss
maternally-inherited Leigh syndrome
MeSH: C536035
maternally-inherited mitochondrial dystonia
Maternally-inherited mitochondrial dystonia is a rare neurological mitochondrial DNA-related disorder characterized clinically by progressive pediatric-onset dystonia with variable degrees of severity
maternally-inherited mitochondrial myopathy
human disease