ZFIN Human Disease: autosomal recessive intellectual developmental disorder 65

OBO ID: DOID:0081226

Term Name:	autosomal recessive intellectual developmental disorder 65		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous or compound heterozygous mutation in the KDM5B gene on chromosome 1q32. https://pubmed.ncbi.nlm.nih.gov/29276005/
References:	OMIM:618109
Ontology:	Human Disease ( DOID:0081226 )

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 65 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KDM5B	kdm5ba kdm5bb	Intellectual developmental disorder, autosomal recessive 65	618109

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None