Disease #00142 (FCAS2 (FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2), OMIM:611762)
| Official abbreviation |
FCAS2 |
| Name |
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2 |
| OMIM ID |
611762 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NLRP12 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-06-16 11:16:19 +00:00 (UTC) |
| Date last edited |
N/A |
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