Disease #03660 (CCHLND (cataracts, congenital, hearing loss, and neurodegeneration (CCHLND)), OMIM:614482)
| Official abbreviation |
CCHLND |
| Name |
cataracts, congenital, hearing loss, and neurodegeneration (CCHLND) |
| OMIM ID |
614482 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC33A1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
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