ZFIN Human Disease: autosomal dominant intellectual developmental disorder 42

OBO ID: DOID:0070072

Term Name:	autosomal dominant intellectual developmental disorder 42		Search Ontology:
Synonyms:	autosomal dominant mental retardation 42 autosomal dominant non-syndromic intellectual disability 42 MRD42
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GNB1 gene on chromosome 1p36.33. https://www.ncbi.nlm.nih.gov/pubmed/27108799
References:	OMIM:616973
Ontology:	Human Disease ( DOID:0070072 )

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 42 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GNB1	gnb1a gnb1b	Intellectual developmental disorder, autosomal dominant 42	616973

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None