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DO Term : hereditary spherocytosis type 2 [DOID:0110917] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTB gene on chromosome 14q23.3.

synonyms:
SPH2,
hereditary spherocytosis 2,
616649,
OMIM:616649,
HS2

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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