Disease #07246 (CAOP (cataract, alopecia, oral mucosal disorder, psoriasis-like syndrome), OMIM:621252)
| Official abbreviation |
CAOP |
| Name |
cataract, alopecia, oral mucosal disorder, psoriasis-like syndrome |
| OMIM ID |
621252 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
MBTPS1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2026-03-20 14:06:24 +01:00 (CET) |
| Date last edited |
N/A |
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