Disease #06414 (EIEE46 (Epileptic encephalopathy, early infantile, 46), OMIM:617162)

Official abbreviation EIEE46
Name Epileptic encephalopathy, early infantile, 46
OMIM ID 617162
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 GRIN2D
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

1 entry on 1 page. Showing entry 1.
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00452321 299118 - - F no ? (unknown) - - - - - EIEE46 Abnormality of movement, Scoliosis, Strabismus, Broad-based gait, Obesity, Paroxysmal bursts of laughter, Intellectual disability, borderline, Anxiety, Cleft palate, Thick eyebrow, Thin upper lip vermilion, Neurodevelopmental delay GRIN2D GRIN2D 1 1 Andreas Laner
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