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Luo-Schoch-Yamamoto Syndrome

Disease ID: disease_node_16482

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DbxrefMIM:619460
SubclassofDOID_0060307
Data SourceDOID
SynonymsLUSYAM
Doid LabelLuo-Schoch-Yamamoto syndrome
Doid DescriptionA autosomal domit intellectual developmental disorder characterized by global developmental delay and impaired intellectual development apparent from infancy that has_material_basis_in heterozygous mutation in the RNF2 gene on chromosome 1q25.
Disease Node Iddisease_node_16482
Doid IdDOID_0070416
LabelLuo-Schoch-Yamamoto Syndrome