OBO ID: DOID:0081186
Term Name: autosomal recessive intellectual developmental disorder 11 Search Ontology:
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 )
OTHER autosomal recessive intellectual developmental disorder 11 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None