ZFIN Human Disease: autosomal dominant intellectual developmental disorder 11

OBO ID: DOID:0070041

Term Name:	autosomal dominant intellectual developmental disorder 11		Search Ontology:
Synonyms:	autosomal dominant mental retardation 11 autosomal dominant non-syndromic intellectual disability 11 MRD11
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the EPB41L1 gene on chromosome 20q11.23. https://www.ncbi.nlm.nih.gov/pubmed/21376300
References:	OMIM:614257
Ontology:	Human Disease ( DOID:0070041 )

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 11 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
EPB41L1		?Intellectual developmental disorder, autosomal dominant 11

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None