Disease Index
9,486 diseasesmelorheostosis with osteopoikilosis
membranoproliferative glomerulonephritis
glomerulonephritis caused by deposits in the kidney glomerular mesangium and basement membrane thickening, activating the complement system and damaging the glomeruli
ICD: N00MeSH: D015432
MEND syndrome
human disease
Mendelian susceptibility to mycobacterial disease
medical condition
mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
MeSH: C535530
mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
infections
mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
infections
mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Mendelian susceptibility to mycobacterial diseases (MSMD) due to complete ISG15 deficiency is a genetic variant of MSMD (see this term) characterized by Bacille Calmette-GuC)rin (BCG) infections
mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
human disease
Meniere's disease
disorder of the inner ear, characterized by potentially severe and incapacitating episodes of vertigo, tinnitus, hearing loss, and a feeling of fullness in the ear
MeSH: D008575
meningeal melanocytoma
Human disease
meningioma
tumor forms from meninges
MeSH: D008579
meningocele
disease
MeSH: D008588
meningococcal meningitis
bacterial meningitis that has material basis in Neisseria meningitidis infection
ICD: A39.0MeSH: D008585
Menke-Hennekam syndrome
medical condition
Menkes disease
Human disease
ICD: E83.0MeSH: D007706
mental retardation and microcephaly with pontine and cerebellar hypoplasia
rare X-linked dominant genetic disorder
MeSH: C567466
mercury poisoning
poisoning caused by mercury chemicals
ICD: T56.1MeSH: D008630
Merkel cell carcinoma
rare and highly aggressive skin cancer
ICD: C44MeSH: D015266
MERRF syndrome
mitochondrial disease
MeSH: D017243
mesenchymal tumor of small intestine
human disease
mesenchymatous palpebral tumor
human disease
mesial temporal lobe epilepsy with hippocampal sclerosis
human disease
mesoaxial synostotic syndactyly with phalangeal reduction
MeSH: C563721
Mesocardia
human disease
mesomelia-synostoses syndrome
MeSH: C537348
mesomelic and rhizo-mesomelic dysplasia
human disease
mesomelic dwarfism-cleft palate-camptodactyly syndrome
medical condition
ICD: Q78.8