familial apolipoprotein C-II deficiency
human disease
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familial apolipoprotein C-II deficiency
Summary
familial apolipoprotein C-II deficiency is a rare disease[1].
Key Facts
- familial apolipoprotein C-II deficiency's instance of is recorded as rare disease[2].
- familial apolipoprotein C-II deficiency's instance of is recorded as class of disease[3].
- familial apolipoprotein C-II deficiency's subclass of is recorded as autosomal recessive disease[4].
- familial apolipoprotein C-II deficiency's subclass of is recorded as familial chylomicronemia syndrome[5].
- familial apolipoprotein C-II deficiency's OMIM ID is recorded as 207750[6].
- familial apolipoprotein C-II deficiency's Disease Ontology ID is recorded as DOID:0111418[7].
- familial apolipoprotein C-II deficiency's Orphanet ID is recorded as 309020[8].
- familial apolipoprotein C-II deficiency's Orphanet ID is recorded as 411[9].
- familial apolipoprotein C-II deficiency's genetic association is recorded as APOC2[10].
- familial apolipoprotein C-II deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_309020[11].
- familial apolipoprotein C-II deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_411[12].
- familial apolipoprotein C-II deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111418[13].
- familial apolipoprotein C-II deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0111418[14].
- familial apolipoprotein C-II deficiency's UMLS CUI is recorded as C0268199[15].
- familial apolipoprotein C-II deficiency's UMLS CUI is recorded as C1720779[16].
- familial apolipoprotein C-II deficiency's ICD-10-CM is recorded as E78.3[17].
- familial apolipoprotein C-II deficiency's Mondo ID is recorded as MONDO_0008810[18].
- familial apolipoprotein C-II deficiency's UniProt disease ID is recorded as DI-01770[19].