atypical glycine encephalopathy
Atypical glycine encephalopathy is a rare form of glycine encephalopathy (GE; see this term) presenting disease onset or clinical manifestations that differ from neonatal or infantile GE
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Summary
atypical glycine encephalopathy is a rare disease[1].
Key Facts
- atypical glycine encephalopathy's instance of is recorded as rare disease[2].
- atypical glycine encephalopathy's instance of is recorded as class of disease[3].
- atypical glycine encephalopathy's subclass of is recorded as glycine encephalopathy[4].
- atypical glycine encephalopathy's OMIM ID is recorded as 617301[5].
- atypical glycine encephalopathy's KEGG ID is recorded as H02419[6].
- atypical glycine encephalopathy's Orphanet ID is recorded as 289863[7].
- atypical glycine encephalopathy's genetic association is recorded as SLC6A9[8].
- atypical glycine encephalopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_289863[9].
- atypical glycine encephalopathy's UMLS CUI is recorded as C4310943[10].
- atypical glycine encephalopathy's UMLS CUI is recorded as C5548198[11].
- atypical glycine encephalopathy's ICD-10-CM is recorded as E72.5[12].
- atypical glycine encephalopathy's Mondo ID is recorded as MONDO_0015010[13].