Disease #06121 (NEDSGA (Neurodevelopmental disorder with or without seizures and gait abnormalities), OMIM:617864)

Official abbreviation NEDSGA
Name Neurodevelopmental disorder with or without seizures and gait abnormalities
OMIM ID 617864
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 GRIA4
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00432974 251198 - - F ? Pakistan - - - - - NEDSGA Agitation, Opisthotonus, Hypertonia, Hyperreflexia, Neurodevelopmental delay, Failure to thrive in infancy, Secundum atrial septal defect, Exaggerated startle response, Glutaric aciduria GRIA4 GRIA4 1 1 Andreas Laner
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