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DO Term : ovarian dysgenesis 10 [DOID:0061014] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A 46 XX gonadal dysgenesis characterized by primary amenorrhea and absent puberty that has_material_basis_in homozygous mutation in the ZSWIM7 gene on chromosome 17p12.

synonyms:
619834,
ODG10,
OMIM:619834

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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