ZFIN Human Disease: autosomal dominant intellectual developmental disorder 48

OBO ID: DOID:0080235

Term Name:	autosomal dominant intellectual developmental disorder 48		Search Ontology:
Synonyms:	autosomal dominant mental retardation 48
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the RAC1 gene on chromosome 7p22. https://pubmed.ncbi.nlm.nih.gov/28886345/
References:	OMIM:617751
Ontology:	Human Disease ( DOID:0080235 )

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 48 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RAC1	rac1b rac1a	Intellectual developmental disorder, autosomal dominant 48	617751

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None