Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 5

Term ID
DOID:0081181
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the NSUN2 gene on chromosome 5p15. https://pubmed.ncbi.nlm.nih.gov/22541559/
References
Ontology
Human Disease   ( DOID:0081181 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models