ZFIN Human Disease: autosomal dominant intellectual developmental disorder 2

OBO ID: DOID:0070032

OBO ID: DOID:0070032

Term Name:	autosomal dominant intellectual developmental disorder 2	Search Ontology:
Synonyms:	autosomal dominant mental retardation 2 autosomal dominant non-syndromic intellectual disability 2 MRD2
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DOCK8 gene on chromosome 9p24. https://www.ncbi.nlm.nih.gov/pubmed/18060736
References:	OMIM:614113
Ontology:	Human Disease ( DOID:0070032 )

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 2 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None