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Human Disease

autosomal recessive intellectual developmental disorder 11

Term ID
DOID:0081186
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in a candidate locus on chromosome 19q, termed MRT11. Haplotype analysis delineated a 5.4-Mb candidate region between SNPs rs2109075 and rs8101149. https://pubmed.ncbi.nlm.nih.gov/21063731/
References
Ontology
Human Disease   ( DOID:0081186 )
Relationships
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Genes Involved
Zebrafish Models