Disease #00700 (JBTS-5 (Joubert syndrome, type 5 (JBTS-5)), OMIM:610188)
| Official abbreviation |
JBTS-5 |
| Name |
Joubert syndrome, type 5 (JBTS-5) |
| OMIM ID |
610188 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CEP290 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|