ZFIN Human Disease: autosomal dominant intellectual developmental disorder 5

OBO ID: DOID:0070035

Term Name:	autosomal dominant intellectual developmental disorder 5		Search Ontology:
Synonyms:	autosomal dominant mental retardation 5 autosomal dominant non-syndromic intellectual disability 5 MRD5
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SYNGAP1 gene on chromosome 6p21.32. https://www.ncbi.nlm.nih.gov/pubmed/19196676
References:	OMIM:612621
Ontology:	Human Disease ( DOID:0070035 )

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 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SYNGAP1	syngap1b syngap1a	Intellectual developmental disorder, autosomal dominant 5	612621

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None