White-Sutton syndrome
autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of POGZ on chromosome 1q21.3
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White-Sutton syndrome
Summary
White-Sutton syndrome is a developmental defect during embryogenesis[1]. It draws 100 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2]
Key Facts
- White-Sutton syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- White-Sutton syndrome's instance of is recorded as rare disease[4].
- White-Sutton syndrome's instance of is recorded as class of disease[5].
- White-Sutton syndrome is a type of autosomal dominant non-syndromic intellectual disability[6].
- White-Sutton syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[7].
- White-Sutton syndrome is a type of genetic syndromic intellectual disability[8].
- White-Sutton syndrome's genetic association is recorded as POGZ[9].
- White-Sutton syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070067[10].
- White-Sutton syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0070067[11].
- White-Sutton syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_468678[12].
- White-Sutton syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
White-Sutton syndrome draws 100 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #128 of 308).[2] It is known by 12 alternative names across languages and contexts.[14]