Disease Index
9,486 diseasesminimal pigment oculocutaneous albinism type 1
MIRAGE syndrome
human disease
Mirhosseini–Holmes–Walton syndrome
human disease
MeSH: C538367
mirror movement disorder
movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs
mirror polydactyly-vertebral segmentation-limbs defects syndrome
medical condition
miscellaneous movement disorder due to genetic neurodegenerative disease
human disease
miscellaneous movement disorder due to neurodegenerative disease
human disease
mismatch repair cancer syndrome
genetic disease
MeSH: C536928
MiT family translocation renal cell carcinoma
Mitchell syndrome
human disease
Mitchell-Riley syndrome
human disease
MeSH: C567570
MITF-related melanoma and renal cell carcinoma predisposition syndrome
human disease
Mitis junctional epidermolysis bullosa
human disease
mitochondrial complex I deficiency
Human disease
MeSH: C537475
mitochondrial complex II deficiency
Human disease
MeSH: C565375
mitochondrial complex III deficiency
mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial respiratory chain complex III
mitochondrial complex III deficiency nuclear type 1
Human disease
mitochondrial complex V (ATP synthase) deficiency
mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex
mitochondrial complex V (ATP synthase) deficiency nuclear type 2
mitochondrial metabolism disease that has material basis in mutation in the TMEM70 gene on chromosome 8q21
MeSH: C567528
mitochondrial complex V (ATP synthase) deficiency nuclear type 3
mitochondrial metabolism disease that has material basis in mutation in the ATP5E gene on chromosome 20q13
mitochondrial complex V (ATP synthase) deficiency nuclear type 4
mitochondrial metabolism disease that has material basis in mutation in the ATP5A1 gene on chromosome 18q
mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
mitochondrial metabolism disease that has material basis in mutation in the ATPAF2 gene on chromosome 17p11
mitochondrial disease
spontaneously occuring or inherited disorder that involves mitochondrial dysfunction
MeSH: D028361
mitochondrial disease with dilated cardiomyopathy
human disease
mitochondrial disease with epilepsy
human disease
mitochondrial disease with eye involvement
human disease
mitochondrial disease with hypertrophic cardiomyopathy
human disease
mitochondrial disease with peripheral neuropathy
human disease
mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes
human disease
mitochondrial DNA deletion syndrome with progressive myopathy
human disease