Disease #02163 (ODG2;POF4 (dysgenesis, ovarian, type 2 (premature ovarian failure, type 4)), OMIM:300510)

Official abbreviation ODG2;POF4
Name dysgenesis, ovarian, type 2 (premature ovarian failure, type 4)
OMIM ID 300510
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BMP15
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-04-07 17:47:55 +02:00 (CEST)

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