OBO ID: DOID:0080493
Term Name: ovarian dysgenesis 1 Search Ontology:
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:
Ontology: Human Disease   (DOID:0080493)
OTHER ovarian dysgenesis 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FSHR Ovarian dysgenesis 1 233300
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None