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Human Disease

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
Ontology
Human Disease   ( DOID:0081185 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models