Disease Index
9,486 diseasesmesomelic dwarfism, Nievergelt type
disease
MeSH: C536120
mesomelic dysplasia, Kantaputra type
Mesomelic dysplasia Kantaputra type (MDK) is a rare skeletal disease characterized by symmetric shortening of the middle segments of limbs and short stature
MeSH: C535547
Mesomelic dysplasia, Savarirayan type
MeSH: C565349
metabolic disease associated with ocular features
human disease
metabolic disease due to other fatty acid oxidation disorder
human disease
metabolic disease involving other neurotransmitter deficiency
human disease
metabolic disease with cataract
human disease
metabolic disease with corneal opacity
human disease
metabolic disease with dementia
human disease
metabolic disease with epilepsy
human disease
metabolic disease with intestinal involvement
metabolic disease that involves the intestine
metabolic disease with macular cherry-red spot
human disease
metabolic disease with pigmentary retinitis
human disease
metabolic dysfunction–associated steatotic liver disease
storing of excess fat in liver cells, not caused by heavy alcohol use
ICD: K76.0MeSH: D065626
metabolic myopathy
group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. The disorders are characterized by muscle dysfunction
metabolic myopathy due to lactate transporter defect
human disease
MeSH: C565449
metabolic neurotransmission anomaly with epilepsy
human disease
metabolic skin disease
Human disease
MeSH: D012875
metachondromatosis
a rare disorder characterized by the presence of both multiple enchondromas and osteochondroma-like lesions
MeSH: C562938
metachromatic leukodystrophy
human disease
MeSH: D007966
metachromatic leukodystrophy, adult form
human disease
metachromatic leukodystrophy, juvenile form
human disease
metachromatic leukodystrophy, late infantile form
human disease
metageria
medical condition
MeSH: C538187
metal transport or utilization disorder with epilepsy
human disease
metaphyseal acroscyphodysplasia
MeSH: C537350
metaphyseal anadysplasia
MeSH: C537351
metaphyseal chondrodysplasia-retinitis pigmentosa syndrome
human disease
MeSH: C565398
metaphyseal chondrodysplasia, Kaitila type
human disease
MeSH: C565400
metaphyseal chondrodysplasia, Spahr type
human disease
MeSH: C537353