Disease #06723 (POBINDS (Poirier-Bienvenu neurodevelopmental syndrome), OMIM:618732)

Official abbreviation POBINDS
Name Poirier-Bienvenu neurodevelopmental syndrome
OMIM ID 618732
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 CSNK2B
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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00408813 196081 - - M no Germany - - - - - POBINDS Seizure, Focal-onset seizure, Neurodevelopmental delay, Delayed speech and language development CSNK2B CSNK2B 1 1 Andreas Laner
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