Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 9/26
- Term ID
- DOID:0081184
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 9.1-Mb region on proximal chromosome 14q between SNPs rs10132585 and rs1278951, termed the MRT9 locus. https://pubmed.ncbi.nlm.nih.gov/21629298/
- References
- Ontology
- Human Disease ( DOID:0081184 )
- is a type of
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Genes Involved
Zebrafish Models