Disease #00669 (USH2C (Usher syndrome,, type IIC (USH2C, GPR98/PDZD7 digenic)), OMIM:605472)
| Official abbreviation |
USH2C |
| Name |
Usher syndrome,, type IIC (USH2C, GPR98/PDZD7 digenic) |
| OMIM ID |
605472 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive, Digenic dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
2 |
| Associated with 2 genes |
GPR98, PDZD7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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