familial apolipoprotein C-II deficiency
http://purl.obolibrary.org/obo/MONDO_0008810
Term info
database cross reference
- OMIM:207750 (Orphanet:309020/e)
- UMLS:C1720779 (Orphanet:309020)
- Orphanet:309020 (OMIM:207750)
- SCTID:33513003 (MONDO:equivalentTo)
- DOID:0111418 (MONDO:equivalentTo)
- UMLS:C0268199 (Orphanet:309020/e)
Subsets
ordo_clinical_subtype
exactMatch
http://linkedlifedata.com/resource/umls/id/C1720779, http://identifiers.org/snomedct/33513003, https://omim.org/entry/207750, http://purl.obolibrary.org/obo/DOID_0111418, http://purl.obolibrary.org/obo/Orphanet_309020, http://linkedlifedata.com/resource/umls/id/C0268199
has exact synonym
hyperlipoproteinemia, type IB, familial apoC-II deficiency, familial apolipoprotein C-II deficiency
has related synonym
C-II Anapolipoproteinemia, hyperlipoproteinemia, type 1B, Apoc2 deficiency, apolipoprotein C-II deficiency
id
MONDO:0008810