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white-sutton syndrome

^ http://www.ebi.ac.uk/efo/EFO_0009079


An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of POGZ on chromosome 1q21.3. [ http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern ]

Synonyms: MRD37, WHSUS, autosomal dominant mental retardation 37

Term info

database cross reference
  • DOID:0070067 (http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern)
term editor

Hannah McLaren