Disease #03558 (DFNB-81;PRLTS-3 (deafness, autosomal recessive, type 81 (DFNB-81, Perrault syndrome, type 3 (PRLTS-3))), OMIM:614129)
| Official abbreviation |
DFNB-81;PRLTS-3 |
| Name |
deafness, autosomal recessive, type 81 (DFNB-81, Perrault syndrome, type 3 (PRLTS-3)) |
| OMIM ID |
614129 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CLPP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
