ZFIN Human Disease: autosomal dominant intellectual developmental disorder 30

OBO ID: DOID:0070060

Term Name:	autosomal dominant intellectual developmental disorder 30		Search Ontology:
Synonyms:	autosomal dominant mental retardation 30 autosomal dominant non-syndromic intellectual disability 30 MRD30
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the ZMYND11 gene on chromosome 10p15.3. https://www.ncbi.nlm.nih.gov/pubmed/25217958
References:	OMIM:616083
Ontology:	Human Disease ( DOID:0070060 )

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 30 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ZMYND11	zmynd11	Intellectual developmental disorder, autosomal dominant 30	616083

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None