Disease #00030 (ODG1 (dysgenesis, ovarian, type 1), OMIM:233300)
Official abbreviation |
ODG1 |
Name |
dysgenesis, ovarian, type 1 |
OMIM ID |
233300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
16 |
Phenotype entries for this disease |
15 |
Associated with 1 gene |
FSHR |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-08-27 15:15:31 +02:00 (CEST) |
Date last edited |
2023-02-08 10:19:37 +01:00 (CET) |
Individuals
|