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Autosomal Domit Intellectual Developmental Disorder 42

Disease ID: disease_node_16485

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DbxrefMIM:616973
SubclassofDOID_0060307
Data SourceDOID
SynonymsMRD42, autosomal dominant mental retardation 42, autosomal dominant non-syndromic intellectual disability 42
Doid Labelautosomal domit intellectual developmental disorder 42
Doid DescriptionAn autosomal domit intellectual developmental disorder that has_material_basis_in an autosomal domit mutation of the GNB1 gene on chromosome 1p36.33.
Disease Node Iddisease_node_16485
Doid IdDOID_0070072
LabelAutosomal Domit Intellectual Developmental Disorder 42