hypoalphalipoproteinemia
metabolic disorder characterized by deficiency of high density (alpha) lipoprotein in the blood
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hypoalphalipoproteinemia
Summary
hypoalphalipoproteinemia is a genetic disease[1].
Key Facts
- hypoalphalipoproteinemia's instance of is recorded as genetic disease[2].
- hypoalphalipoproteinemia's instance of is recorded as rare disease[3].
- hypoalphalipoproteinemia's instance of is recorded as class of disease[4].
- hypoalphalipoproteinemia's subclass of is recorded as hypolipoproteinemia[5].
- hypoalphalipoproteinemia's MeSH descriptor ID is recorded as D052456[6].
- hypoalphalipoproteinemia's OMIM ID is recorded as 604091[7].
- hypoalphalipoproteinemia's ICD-9 ID is recorded as 272.5[8].
- hypoalphalipoproteinemia's ICD-10 ID is recorded as E78.6[9].
- hypoalphalipoproteinemia's KEGG ID is recorded as H00930[10].
- hypoalphalipoproteinemia's MeSH tree code is recorded as C16.320.565.398.500.330[11].
- hypoalphalipoproteinemia's MeSH tree code is recorded as C18.452.584.500.875.330[12].
- hypoalphalipoproteinemia's MeSH tree code is recorded as C18.452.648.398.500.330[13].
- hypoalphalipoproteinemia's MeSH tree code is recorded as C18.452.584.563.500.330[14].
- hypoalphalipoproteinemia's eMedicine ID is recorded as 127943[15].
- hypoalphalipoproteinemia's Orphanet ID is recorded as 31153[16].
- hypoalphalipoproteinemia's NCI Thesaurus ID is recorded as C84774[17].
- hypoalphalipoproteinemia's health specialty is recorded as endocrinology[18].
- hypoalphalipoproteinemia's genetic association is recorded as ABCA1[19].
- hypoalphalipoproteinemia's genetic association is recorded as APOA1[20].
- hypoalphalipoproteinemia's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003233[21].
- hypoalphalipoproteinemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_31153[22].
- hypoalphalipoproteinemia's UMLS CUI is recorded as C0473527[23].
- hypoalphalipoproteinemia's UMLS CUI is recorded as C0151691[24].
- hypoalphalipoproteinemia's Medical Dictionary for Regulatory Activities ID is recorded as 10024626[25].
- hypoalphalipoproteinemia's Human Phenotype Ontology ID is recorded as HP:0003233[26].