ethylmalonic encephalopathy

Summary

ethylmalonic encephalopathy is a developmental defect during embryogenesis^[1]. It is known by 9 alternative names across languages and contexts.^[2]

Key Facts

• ethylmalonic encephalopathy's instance of is recorded as developmental defect during embryogenesis^[3].
• ethylmalonic encephalopathy's instance of is recorded as rare disease^[4].
• ethylmalonic encephalopathy's instance of is recorded as class of disease^[5].
• ethylmalonic encephalopathy is a type of mitochondrial disease^[6].
• ethylmalonic encephalopathy is a type of unspecified mitochondrial disorder^[7].
• ethylmalonic encephalopathy is a type of genetic disease^[8].
• ethylmalonic encephalopathy's symptoms and signs is recorded as diarrhea^[9].
• ethylmalonic encephalopathy's health specialty is recorded as neurology^[10].
• ethylmalonic encephalopathy's genetic association is recorded as ETHE1^[11].
• ethylmalonic encephalopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060640^[12].
• ethylmalonic encephalopathy's exact match is recorded as http://identifiers.org/doid/DOID:0060640^[13].
• ethylmalonic encephalopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_51188^[14].
• ethylmalonic encephalopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine^[15].

Why It Matters

ethylmalonic encephalopathy is known by 9 alternative names across languages and contexts.^[2]