Disease #07161 (NEDLBAS (neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures), OMIM:620292)

Official abbreviation NEDLBAS
Name neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures
OMIM ID 620292
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene EIF2C1
Associated tissues -
Disease features -
Remarks -
Date created 2025-03-31 12:04:35 +02:00 (CEST)
Date last edited N/A

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