Disease #02169 (POF2B (ovarian failure, premature, type 2B (POF-2B)), OMIM:300604)

Official abbreviation POF2B
Name ovarian failure, premature, type 2B (POF-2B)
OMIM ID 300604
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene POF1B
Associated tissues -
Disease features -
Remarks -