Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 35
- Term ID
- DOID:0081201
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 12.2-Mb region on chromosome 17q21.31-q22 between SNPs rs4792947 and rs11079258. https://pubmed.ncbi.nlm.nih.gov/20950399/
- References
- Ontology
- Human Disease ( DOID:0081201 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models