ZFIN Human Disease: autosomal dominant intellectual developmental disorder 53

OBO ID: DOID:0080228

Term Name:	autosomal dominant intellectual developmental disorder 53		Search Ontology:
Synonyms:	autosomal dominant mental retardation 53
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the CAMK2A gene on chromosome 5q32. https://pubmed.ncbi.nlm.nih.gov/29100089/
References:	OMIM:617798
Ontology:	Human Disease ( DOID:0080228 )

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 53 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CAMK2A	camk2a	Intellectual developmental disorder, autosomal dominant 53	617798

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None