Ovarian dysgenesis 9

Preferred Label : Ovarian dysgenesis 9;

Symbol : ODG9;

Type : Phenotype, molecular basis known;

Prefixed ID : #619665;

Origin ID

619665;

UMLS CUI

C5562046;

Genes related to phenotype
- Scaffolding protein involved in dna repair [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Decreased antimullerian hormone level [HPO term]
- Decreased serum estradiol [HPO term]
- Delayed puberty [HPO term]
- Delayed skeletal maturation [HPO term]
- Elevated circulating follicle stimulating hormone level [HPO term]
- Elevated circulating luteinizing hormone level [HPO term]
- Hypoplasia of the ovary [HPO term]
- Hypoplasia of the uterus [HPO term]
- Juvenile onset [HPO term]
- Premature ovarian insufficiency [HPO term]
- Primary amenorrhea [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]