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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