Disease #02413 (USH1F (Usher syndrome, type 1F (USH-1F)), OMIM:602083)
Official abbreviation |
USH1F |
Name |
Usher syndrome, type 1F (USH-1F) |
OMIM ID |
602083 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
PCDH15 |
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
|