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DO Term : familial hypobetalipoproteinemia 2 [DOID:0111061] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypobetalipoproteinemia that has_material_basis_in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31.

synonyms:
FHBL2,
605019,
combined familial hypolipidemia,
OMIM:605019

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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