Disease #06127 (IDDMSSD (Intellectual developmental disorder with macrocephaly, seizures, and speech delay), OMIM:618158)
| Official abbreviation |
IDDMSSD |
| Name |
Intellectual developmental disorder with macrocephaly, seizures, and speech delay |
| OMIM ID |
618158 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PAK1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
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