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DO Term : primary ovarian insufficiency 9 [DOID:0080866] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A primary ovarian insufficiency that has_material_basis_in compound heterozygous mutation in the HFM1 gene on chromosome 1p22.

synonyms:
OMIM:615724,
615724

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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