Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 30
- Term ID
- DOID:0081195
- Synonyms
-
- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 22-Mb region on proximal chromosome 6q between SNPs rs4612125 and rs285651. https://pubmed.ncbi.nlm.nih.gov/21629298/
- References
- Ontology
- Human Disease ( DOID:0081195 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models