Disease #06382 (NEDBAF (Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies), OMIM:618577)
Official abbreviation |
NEDBAF |
Name |
Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies |
OMIM ID |
618577 |
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 |
RAC3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|