Disease #05988 (IDDSELD (intellectual developmental disorder with seizures and language delay (IDDSELD)), OMIM:619000)
| Official abbreviation |
IDDSELD |
| Name |
intellectual developmental disorder with seizures and language delay (IDDSELD) |
| OMIM ID |
619000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SETD1B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-11-19 09:17:25 +01:00 (CET) |
| Date last edited |
N/A |
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