WormMine: DiseaseOntology DOID:3145 hyperlipoproteinemia type III 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.

1 Ontology

• Name: Disease Ontology

7 Parents

Identifier	Name	Description
DOID:4	disease	A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:0014667	disease of metabolism	A disease that involving errors in metabolic processes of building or degradation of molecules.
DOID:630	genetic disease	A disease that has_material_basis_in genetic variations in the human genome.
DOID:655	inherited metabolic disorder	A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality.
DOID:3146	lipid metabolism disorder	An inherited metabolic disorder that involves the creation and degradation of lipids.
DOID:1168	familial hyperlipidemia
DOID:3145	hyperlipoproteinemia type III	A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13.

6 Relations

Relationship	Parent Term . Identifier	Child Term . Identifier
is_a	DOID:1168	DOID:3145
is_a	DOID:655	DOID:3145
is_a	DOID:0014667	DOID:3145
is_a	DOID:4	DOID:3145
is_a	DOID:630	DOID:3145
is_a	DOID:3146	DOID:3145

4 Synonyms

• Name: carbohydrate induced hyperlipemia
• Type: synonym

• Name: familial hypercholesterolaemia with hyperlipaemia
• Type: synonym

• Name: familial type 3 hyperlipoproteinemia
• Type: synonym

• Name: Remnant hyperlipidemia
• Type: synonym