ZFIN Human Disease: autosomal dominant intellectual developmental disorder 3

OBO ID: DOID:0070033

Term Name:	autosomal dominant intellectual developmental disorder 3		Search Ontology:
Synonyms:	autosomal dominant mental retardation 3 autosomal dominant non-syndromic intellectual disability 3 MRD3
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CDH15 gene on chromosome 16q24.3. https://www.ncbi.nlm.nih.gov/pubmed/19012874
References:	OMIM:612580
Ontology:	Human Disease ( DOID:0070033 )

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 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CDH15	cdh15	Intellectual developmental disorder, autosomal dominant 3	612580

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None