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Autosomal Domit Intellectual Developmental Disorder 10

Disease ID: disease_node_16513

Connections displayed (default: 10).
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DbxrefMIM:614256
SubclassofDOID_0060307
Data SourceDOID
SynonymsMRD10, autosomal dominant mental retardation 10, autosomal dominant non-syndromic intellectual disability 10
Doid Labelautosomal domit intellectual developmental disorder 10
Doid DescriptionAn autosomal domit intellectual developmental disorder that has_material_basis_in an autosomal domit mutation of the CACNG2 gene on chromosome 22q12.3.
Disease Node Iddisease_node_16513
Doid IdDOID_0070040
LabelAutosomal Domit Intellectual Developmental Disorder 10