Disease #00242 (CFSMR (dysmorphism, craniofacial, skeletal anomalies, and mental retardation syndrome (CFSMR)), OMIM:614132)
| Official abbreviation |
CFSMR |
| Name |
dysmorphism, craniofacial, skeletal anomalies, and mental retardation syndrome (CFSMR) |
| OMIM ID |
614132 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TMCO1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-10-11 20:22:53 +02:00 (CEST) |
| Date last edited |
N/A |
|
