Disease #02163 (ODG-2 (dysgenesis, ovarian, type 2 (ODG-2, ovarian failure, premature type 4 (POF-4))), OMIM:300510)

Official abbreviation ODG-2
Name dysgenesis, ovarian, type 2 (ODG-2, ovarian failure, premature type 4 (POF-4))
OMIM ID 300510
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene BMP15
Associated tissues -
Disease features -
Remarks -