autosomal recessive intellectual developmental disorder 10/20

Term ID

DOID:0081185

Synonyms

Definition

An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 21.7-Mb region in the pericentromeric region of chromosome 16 between SNPs rs7197568 and rs7197227, termed the MRT20 locus. https://pubmed.ncbi.nlm.nih.gov/21629298/

References

• OMIM:611096

Ontology

Human Disease   ( DOID:0081185 )