Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 10/20
- Term ID
- DOID:0081185
- Synonyms
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- 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 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models