Disease #06243 (IDDSFTA (Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities), OMIM:618092)
Official abbreviation |
IDDSFTA |
Name |
Intellectual developmental disorder with dysmorphic facies, speech delay, and T-cell abnormalities |
OMIM ID |
618092 |
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 |
BCL11B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|