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DO Term : congenital nonspherocytic hemolytic anemia 8 [DOID:0051007] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the UMPH1 gene (NT5C3A) on chromosome 7p14.

synonyms:
OMIM:266120,
266120

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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