ZFIN Human Disease: autosomal dominant intellectual developmental disorder 22

OBO ID: DOID:0070052

Term Name:	autosomal dominant intellectual developmental disorder 22		Search Ontology:
Synonyms:	autosomal dominant mental retardation 22 autosomal dominant non-syndromic intellectual disability 22 MRD22
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the ZBTB18 gene on chromosome 1q44. https://www.ncbi.nlm.nih.gov/pubmed/24193349
References:	OMIM:612337
Ontology:	Human Disease ( DOID:0070052 )

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 22 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ZBTB18	zbtb18	Intellectual developmental disorder, autosomal dominant 22	612337

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None