Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 82

Term ID
DOID:0060947
Synonyms
Definition
An autosomal recessive intellectual developmental disorder characterized by global developmental delay with motor and speech delay, variably impaired intellectual development, and behavioral abnormalities has_material_basis_in homozygous mutation in the NSUN6 gene on chromosome 10p12. https://pubmed.ncbi.nlm.nih.gov/37226891/
References
Ontology
Human Disease   ( DOID:0060947 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models