Disease #05904 (DEDSM (developmental delay and seizures, with/without movement abnormalities (DEDSM)), OMIM:617836)
| Official abbreviation |
DEDSM |
| Name |
developmental delay and seizures, with/without movement abnormalities (DEDSM) |
| OMIM ID |
617836 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
DHDDS |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-03-03 09:54:40 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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