Disease #05334 (CSCF (cardiospondylocarpofacial syndrome (CSCF)), OMIM:157800)
| Official abbreviation |
CSCF |
| Name |
cardiospondylocarpofacial syndrome (CSCF) |
| OMIM ID |
157800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
MAP3K7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-10-21 23:51:06 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|