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DO Term : autosomal recessive hypercholesterolemia [DOID:0090105] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A familial hypercholesterolemia that is characterized by very high levels of low-density lipoprotein (LDL) cholesterol (usually above 400 mg/dl) and increased risk of premature atherosclerotic cardiovascular disease, and has_material_basis_in autosomal recessive homozygous mutation in the low density lipoprotein receptor adaptor protein 1 gene (LDLRAP1) on chromosome 1p36.
  • synonyms:
  • FHCB2,
  • ARH1,
  • familial autosomal recessive hypercholesterolemia,
  • ARH2,
  • ICD10CM:E78.0,
  • FHCB1,
  • OMIM:603813,
  • ARH,
  • 603813,
  • autosomal recessive hypercholesterolemia 1,
  • autosomal recessive hypercholesterolemia 2,
  • ORDO:391665
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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