Disease #00532 (CCMS (cerebro-cosot-mandibular syndrome (CCMS)), OMIM:117650)
| Official abbreviation |
CCMS |
| Name |
cerebro-cosot-mandibular syndrome (CCMS) |
| OMIM ID |
117650 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
SNRPB |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-21 11:44:36 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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