Disease #06937 (NEDHYDF (neurodevelopmental disorder with hypotonia and dysmorphic facies), OMIM:619503)

Official abbreviation NEDHYDF
Name neurodevelopmental disorder with hypotonia and dysmorphic facies
OMIM ID 619503
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GNB2
Associated tissues -
Disease features -
Remarks -
Date created 2022-04-26 19:55:01 +02:00 (CEST)
Date last edited N/A

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