ZFIN Human Disease: autosomal dominant intellectual developmental disorder 23

OBO ID: DOID:0070053

Term Name:	autosomal dominant intellectual developmental disorder 23		Search Ontology:
Synonyms:	autosomal dominant mental retardation 23 autosomal dominant non-syndromic intellectual disability 23 MRD23
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SETD5 gene on chromosome 3p25.3. https://www.ncbi.nlm.nih.gov/pubmed/24680889
References:	OMIM:615761
Ontology:	Human Disease ( DOID:0070053 )

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 23 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SETD5	setd5	Intellectual developmental disorder, autosomal dominant 23	615761

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None