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
|