Term Name: ovarian dysgenesis 1
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.
Ontology: Human Disease [DOID:0080493]   ( DOID:0080493 )

Relationships
is a type of: 46 XX gonadal dysgenesis autosomal recessive disease