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

1 entry on 1 page. Showing entry 1.
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00358802 176266 - - F ? Germany - - - - - DEDSM (+) Seizure,(+) Intellectual disability, mild,(+) Gait ataxia,(+) Generalized-onset seizure / Epilepsy since the 13th month, with generalised tonic-clonic seizures, generalised frequent or continuous myoclonias, proged ataxia, reduced intelligence, psychotic episodes. DHDDS DHDDS 1 1 Andreas Laner
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