ZFIN Human Disease: autosomal recessive intellectual developmental disorder 67

OBO ID: DOID:0081228

Term Name:	autosomal recessive intellectual developmental disorder 67		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation or compound heterozygous mutation in the EIF3F gene on chromosome 11p15. https://pubmed.ncbi.nlm.nih.gov/30409806/
References:	OMIM:618295
Ontology:	Human Disease ( DOID:0081228 )

Relationships

is a type of:	autosomal recessive intellectual developmental disorder autosomal recessive intellectual developmental disorder Show first 5 Terms

OTHER autosomal recessive intellectual developmental disorder 67 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
EIF3F	eif3f	Intellectual developmental disorder, autosomal recessive 67	618295

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None