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
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