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DO Term : hereditary spherocytosis type 5 [DOID:0110920] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spherocytosis that has_material_basis_in a mutation of the EPB42 gene on chromosome 15q15.2.

synonyms:
hereditary spherocytosis 5,
SPH5,
612690,
HS5,
OMIM:612690

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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