familial hypobetalipoproteinemia 2
hypobetalipoproteinemia that has material basis in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31
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familial hypobetalipoproteinemia 2
Summary
familial hypobetalipoproteinemia 2 is a class of disease[1].
Key Facts
- familial hypobetalipoproteinemia 2's instance of is recorded as class of disease[2].
- familial hypobetalipoproteinemia 2's subclass of is recorded as hypobetalipoproteinemia[3].
- familial hypobetalipoproteinemia 2's MeSH descriptor ID is recorded as C565732[4].
- familial hypobetalipoproteinemia 2's OMIM ID is recorded as 605019[5].
- familial hypobetalipoproteinemia 2's OMIM ID is recorded as 605019[6].
- familial hypobetalipoproteinemia 2's Disease Ontology ID is recorded as DOID:0111061[7].
- familial hypobetalipoproteinemia 2's Orphanet ID is recorded as 426[8].
- familial hypobetalipoproteinemia 2's genetic association is recorded as ANGPTL3[9].
- familial hypobetalipoproteinemia 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111061[10].
- familial hypobetalipoproteinemia 2's exact match is recorded as http://identifiers.org/doid/DOID:0111061[11].
- familial hypobetalipoproteinemia 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_426[12].
- familial hypobetalipoproteinemia 2's UMLS CUI is recorded as C1857970[13].
- familial hypobetalipoproteinemia 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- familial hypobetalipoproteinemia 2's Mondo ID is recorded as MONDO_0011505[15].
- familial hypobetalipoproteinemia 2's UniProt disease ID is recorded as DI-03014[16].