Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	APOLIPOPROTEIN C-II DEFICIENCY
Synonyms	HYPERLIPOPROTEINEMIA, TYPE IB
ID	http://purl.bioontology.org/ontology/OMIM/207750
altLabel	HYPERLIPOPROTEINEMIA, TYPE IB C-II ANAPOLIPOPROTEINEMIA APOC2 DEFICIENCY
cui	C1720779
Gene Locus	19q13.2
Gene Symbol	APOC2
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU014443 http://purl.bioontology.org/ontology/OMIM/MTHU014440 http://purl.bioontology.org/ontology/OMIM/MTHU027673 http://purl.bioontology.org/ontology/OMIM/MTHU014438 http://purl.bioontology.org/ontology/OMIM/MTHU001744 http://purl.bioontology.org/ontology/OMIM/MTHU036371 http://purl.bioontology.org/ontology/OMIM/MTHU002090 http://purl.bioontology.org/ontology/OMIM/MTHU003881 http://purl.bioontology.org/ontology/OMIM/MTHU014437 http://purl.bioontology.org/ontology/OMIM/MTHU014441 http://purl.bioontology.org/ontology/OMIM/MTHU014439
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	207750
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	APOLIPOPROTEIN C-II DEFICIENCY
tui	T047

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/D008072	Medical Subject Headings	CUI