Disease #05460 (USH1B (Usher syndrome, type Ib (USH-1B)), OMIM:276900)
Official abbreviation |
USH1B |
Name |
Usher syndrome, type Ib (USH-1B) |
OMIM ID |
276900 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
537 |
Phenotype entries for this disease |
536 |
Associated with 1 gene |
MYO7A |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2018-07-17 16:02:34 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|