ZFIN Human Disease: autosomal dominant intellectual developmental disorder 13

OBO ID: DOID:0070043

Term Name:	autosomal dominant intellectual developmental disorder 13		Search Ontology:
Synonyms:	autosomal dominant mental retardation 13 autosomal dominant non-syndromic intellectual disability 13 mental retardation, autosomal dominant 13, with neuronal migration defects MRD13
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DYNC1H1 gene on chromosome 14q32.31. https://www.ncbi.nlm.nih.gov/pubmed/21076407
References:	OMIM:614563
Ontology:	Human Disease ( DOID:0070043 )

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 13 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DYNC1H1	dync1h1	Cortical dysplasia, complex, with other brain malformations 13	614563

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None