Disease #02633 (CINCA;CAPS3 (CINCA syndrome (CINCCA, cryopyrin-associted periodic syndrome type 3 (CAPS3))), OMIM:607115)
| Official abbreviation |
CINCA;CAPS3 |
| Name |
CINCA syndrome (CINCCA, cryopyrin-associted periodic syndrome type 3 (CAPS3)) |
| OMIM ID |
607115 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NLRP3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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