Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 23
- Term ID
- DOID:0081196
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 45.6-Mb interval in the pericentromeric region of chromosome 11 between SNPs rs604518 and rs10899421. https://pubmed.ncbi.nlm.nih.gov/21629298/
- References
- Ontology
- Human Disease ( DOID:0081196 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models