Disease #06382 (NEDBAF (Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies), OMIM:618577)

Official abbreviation NEDBAF
Name Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies
OMIM ID 618577
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 RAC3
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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00400075 - - - F - - - - - - - NEDBAF DD/ID; dysmorphic features; seizures; white matter involvement RAC3 RAC3 1 1 Marcello Scala
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