familial hypobetalipoproteinemia 1
hypobetalipoproteinemia that has material basis in mutation in the APOB gene on chromosome 2p24
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familial hypobetalipoproteinemia 1
Summary
familial hypobetalipoproteinemia 1 is a class of disease[1].
Key Facts
- familial hypobetalipoproteinemia 1's instance of is recorded as class of disease[2].
- familial hypobetalipoproteinemia 1's subclass of is recorded as hypobetalipoproteinemia[3].
- familial hypobetalipoproteinemia 1's OMIM ID is recorded as 615558[4].
- familial hypobetalipoproteinemia 1's OMIM ID is recorded as 615558[5].
- familial hypobetalipoproteinemia 1's Disease Ontology ID is recorded as DOID:0111062[6].
- familial hypobetalipoproteinemia 1's Orphanet ID is recorded as 426[7].
- familial hypobetalipoproteinemia 1's genetic association is recorded as APOB[8].
- familial hypobetalipoproteinemia 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111062[9].
- familial hypobetalipoproteinemia 1's exact match is recorded as http://identifiers.org/doid/DOID:0111062[10].
- familial hypobetalipoproteinemia 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_426[11].
- familial hypobetalipoproteinemia 1's UMLS CUI is recorded as CN182502[12].
- familial hypobetalipoproteinemia 1's UMLS CUI is recorded as C1862596[13].
- familial hypobetalipoproteinemia 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- familial hypobetalipoproteinemia 1's Mondo ID is recorded as MONDO_0014252[15].
- familial hypobetalipoproteinemia 1's UniProt disease ID is recorded as DI-01587[16].