ZFIN Human Disease: autosomal dominant intellectual developmental disorder 52

OBO ID: DOID:0080231

Term Name:	autosomal dominant intellectual developmental disorder 52		Search Ontology:
Synonyms:	autosomal dominant mental retardation 52
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the ASH1L gene on chromosome 1q22. https://pubmed.ncbi.nlm.nih.gov/23033978/
References:	OMIM:617796
Ontology:	Human Disease ( DOID:0080231 )

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 52 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ASH1L	ash1l	Intellectual developmental disorder, autosomal dominant 52	617796

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None