MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations. [ Orphanet:550 ]
Term information
- ICD10:G71.3 (Orphanet:550)
- MESH:D017241 (Orphanet:550)
- SCTID:39925003 (MONDO:equivalentTo)
- UMLS:C0162671 (Orphanet:550)
- ICD9:277.87 (i2s)
- Orphanet:550 (OMIM:540000)
- OMIM:540000 (Orphanet:550)
- DOID:3687 (MONDO:equivalentTo)
- NCIT:C84885 (MONDO:equivalentTo)
- MedDRA:10053872 (Orphanet:550)
- GARD:0007009 (Orphanet-shared)
- ICD10:E88.41 (MONDO:equivalentTo)
ordo_disease
MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations.
http://identifiers.org/meddra/10053872
http://purl.obolibrary.org/obo/DOID_3687
http://linkedlifedata.com/resource/umls/id/C0162671
http://identifiers.org/mesh/D017241
http://purl.obolibrary.org/obo/NCIT_C84885
http://identifiers.org/snomedct/39925003
http://identifiers.org/omim/540000
http://www.orpha.net/ORDO/Orphanet_550
mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes
mitochondrial encephalomyopathy, lactic acidosis and stroke
mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
MELAS syndrome
mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
Term relations
- neurometabolic disease
- mitochondrial disease with eye involvement
- syndromic genetic deafness
- mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA
- mitochondrial disease with hypertrophic cardiomyopathy
- mitochondrial disease with peripheral neuropathy
- mitochondrial disease with epilepsy
- mitochondrial encephalomyopathy
- mitochondrial disease with dilated cardiomyopathy