This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration. This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration.

Gand Syndrome

Disease ID: disease_node_16509

Connections displayed (default: 10).
Loading graph...

DbxrefMIM:615074
SubclassofDOID_0060307
Data SourceDOID
SynonymsMRD18, autosomal dominant intellectual developmental disorder 18, autosomal dominant mental retardation 18, autosomal dominant non-syndromic intellectual disability 18
Doid LabelGAND syndrome
Doid DescriptionAn autosomal domit intellectual developmental disorder that is characterized by global developmental delay apparent from infancy, with motor delay and moderate to severely impaired intellectual development and that has_material_basis_in an autosomal domit mutation of the GATAD2B gene on chromosome 1q21.3.
Disease Node Iddisease_node_16509
Doid IdDOID_0070048
LabelGand Syndrome