Disease #05968 (NEDASB (neurodevelopmental disorder with/without autistic features and/or structural brain abnormalities (NEDASB)), OMIM:618859)

Official abbreviation NEDASB
Name neurodevelopmental disorder with/without autistic features and/or structural brain abnormalities (NEDASB)
OMIM ID 618859
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 NOVA2
Associated tissues -
Disease features -
Remarks -
Date created 2021-09-08 13:46:58 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00404287 - - - - - - - - - - - NEDASB DD/ID, ASD, ADHD, stereotyped movements, ataxia, facial dysmorphism - NOVA2 1 1 Marcello Scala
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