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

• OMIM:614208

Ontology

Human Disease   ( DOID:0081189 )