OBO ID: DOID:0070067
Term Name: White-Sutton syndrome Search Ontology:
Synonyms:
  • autosomal dominant mental retardation 37
  • MRD37
  • WHSUS
Definition: An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of POGZ on chromosome 1q21.3. https://www.ncbi.nlm.nih.gov/pubmed/25533962
References:
Ontology: Human Disease   (DOID:0070067)
OTHER White-Sutton syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
POGZ White-Sutton syndrome 616364
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None