Visualize
Metadata
DOID 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

Relationships

is_a 46 XX gonadal dysgenesis

Add an item to the term tracker