Disease #07073 (NEDEGE (neurodevelopmental disorder with or without early-onset generalized epilepsy), OMIM:619157)

Official abbreviation NEDEGE
Name neurodevelopmental disorder with or without early-onset generalized epilepsy
OMIM ID 619157
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 NBEA
Associated tissues -
Disease features -
Remarks -
Date created 2024-03-16 11:48:42 +01:00 (CET)
Date last edited N/A


Individuals

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00462236 200654 - - M no ? (unknown) - - - - - NEDEGE Global developmental delay, Slurred speech NBEA NBEA 1 1 Andreas Laner
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