ZFIN Human Disease: White-Sutton syndrome

OBO ID: DOID:0070067

Term Name:	White-Sutton syndrome		Search Ontology:
Synonyms:	autosomal dominant mental retardation 37 MRD37 WHSUS
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the POGZ gene on chromosome 1q21.3. https://www.ncbi.nlm.nih.gov/pubmed/25533962
References:	OMIM:616364
Ontology:	Human Disease ( DOID:0070067 )

Relationships

is a type of:	autosomal dominant intellectual developmental disorder autosomal dominant intellectual developmental disorder Show first 5 Terms

OTHER White-Sutton syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
POGZ	pogzb pogza	White-Sutton syndrome	616364

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None