ZFIN Human Disease: autosomal dominant intellectual developmental disorder 41

OBO ID: DOID:0070071

Term Name:	autosomal dominant intellectual developmental disorder 41		Search Ontology:
Synonyms:	autosomal dominant mental retardation 41 autosomal dominant non-syndromic intellectual disability 41 MRD41
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the TBL1XR1 gene on chromosome 3q26.32. https://www.ncbi.nlm.nih.gov/pubmed/25102098
References:	OMIM:616944
Ontology:	Human Disease ( DOID:0070071 )

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 41 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TBL1XR1	tbl1xr1b tbl1xr1a	Intellectual developmental disorder, autosomal dominant 41	616944

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None