Disease #06379 (NEDCFSA (Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities), OMIM:618505)
| Official abbreviation |
NEDCFSA |
| Name |
Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities |
| OMIM ID |
618505 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
KDM6B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|