Visualize Submit Comment

Metadata
ID	DOID:0080493
Name	ovarian dysgenesis 1
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
Xrefs	OMIM:233300
Parent Relationships	is_a 46 XX gonadal dysgenesis is_a autosomal recessive disease