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DO Term : hyperlipoproteinemia type III [DOID:3145] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13.

synonyms:
617347,
familial type 3 hyperlipoproteinemia,
UMLS_CUI:C0020479,
Remnant hyperlipidemia,
OMIM:617347,
familial hypercholesterolaemia with hyperlipaemia,
carbohydrate induced hyperlipemia,
NCI:C34710,
SNOMEDCT_US_2023_03_01:42569002,
MESH:D006952

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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