Disease #05962 (NEDAUS (neurodevelopmental disorder with/without autism or seizures), OMIM:619239)

Official abbreviation NEDAUS
Name neurodevelopmental disorder with/without autism or seizures
OMIM ID 619239
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CUL3
Associated tissues -
Disease features -
Remarks -
Date created 2021-08-06 18:44:10 +02:00 (CEST)
Date last edited 2024-12-11 11:24:27 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00408112 194279 - - M likely Germany - - - - - NEDAUS Intellectual disability, Autistic behavior, Behavioral abnormality CUL3 CUL3 1 1 Andreas Laner
00458256 311715 - - M no Germany - - - - - NEDAUS Global developmental delay, Failure to thrive CUL3 CUL3 1 1 Andreas Laner
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