ZFIN Human Disease: autosomal dominant intellectual developmental disorder 1

OBO ID: DOID:0070031

Term Name:	autosomal dominant intellectual developmental disorder 1		Search Ontology:
Synonyms:	autosomal dominant mental retardation 1 autosomal dominant non-syndromic intellectual disability 1 MRD1
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the MBD5 gene on chromosome 2q23.1. https://www.ncbi.nlm.nih.gov/pubmed/21981781
References:	OMIM:156200
Ontology:	Human Disease ( DOID:0070031 )

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 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MBD5	mbd5	Intellectual developmental disorder, autosomal dominant 1	156200

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None