Disease #03762 (USH1J (Usher syndrome, type 1J (USH1J)), OMIM:614869)
Official abbreviation |
USH1J |
Name |
Usher syndrome, type 1J (USH1J) |
OMIM ID |
614869 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
CIB2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-11-11 09:54:40 +01:00 (CET) |
Individuals
|