Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 16

Term ID
DOID:0081189
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in a 23.52-Mb region of homozygosity on chromosome 9p23-p13.3 between rs10738277 and rs12376565, designated MRT16. https://pubmed.ncbi.nlm.nih.gov/20345473/
References
Ontology
Human Disease   ( DOID:0081189 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models