ovarian dysgenesis 1

Term ID

DOID:0080493

Synonyms

Definition

A 46 XX gonadal dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16. https://www.omim.org/entry/233300

References

• OMIM:233300

Ontology

Human Disease   ( DOID:0080493 )