ZFIN Human Disease: autosomal dominant intellectual developmental disorder 29

OBO ID: DOID:0070059

Term Name:	autosomal dominant intellectual developmental disorder 29		Search Ontology:
Synonyms:	autosomal dominant mental retardation 29 autosomal dominant non-syndromic intellectual disability 29 MRD29
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SETBP1 gene on chromosome 18q12.3. https://www.ncbi.nlm.nih.gov/pubmed/25217958
References:	OMIM:616078
Ontology:	Human Disease ( DOID:0070059 )

Relationships

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

OTHER autosomal dominant intellectual developmental disorder 29 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SETBP1	setbp1	Intellectual developmental disorder, autosomal dominant 29	616078

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None