Disease #05186 (POF17 (ovarian failure, premature, type 17), OMIM:619146)

Official abbreviation POF17
Name ovarian failure, premature, type 17
OMIM ID 619146
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene XRCC2
Associated tissues -
Disease features -
Remarks -