Disease #06768 (DEDDFA (Developmental delay with or without dysmorphic facies and autism), OMIM:618454)
Official abbreviation |
DEDDFA |
Name |
Developmental delay with or without dysmorphic facies and autism |
OMIM ID |
618454 |
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 |
TRRAP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|