Disease #06675 (NEDLBA (Neurodevelopmental disorder and language delay with or without structural brain abnormalities), OMIM:618354)

Official abbreviation NEDLBA
Name Neurodevelopmental disorder and language delay with or without structural brain abnormalities
OMIM ID 618354
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene PPP2CA
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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00401308 - - - F no Italy - - - - - NEDLBA - SHANK2 SHANK2 1 1 Alessandra Renieri
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