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Human Disease
autosomal recessive intellectual developmental disorder 16
- Term ID
- DOID:0081189
- Synonyms
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- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in a 23.52-Mb region of homozygosity on chromosome 9p23-p13.3 between rs10738277 and rs12376565, designated MRT16. https://pubmed.ncbi.nlm.nih.gov/20345473/
- References
- Ontology
- Human Disease ( DOID:0081189 )
- is a type of
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Genes Involved
Zebrafish Models