Disease #07167 (DEDISB (developmental delay, impaired speech, and behavioral abnormalities, with/without seizures), OMIM:619964)
Official abbreviation |
DEDISB |
Name |
developmental delay, impaired speech, and behavioral abnormalities, with/without seizures |
OMIM ID |
619964 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ARFGEF1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2025-06-19 11:09:47 +02:00 (CEST) |
Date last edited |
N/A |
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