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Concept information

Deletion of part of chromosome 21 (disorder) > Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder)
Clinical finding (finding) > disease > Genetic disease > Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome (disorder) > Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder)

Preferred term

Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder)  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Finding site

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/783619003

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