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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)
... > Clinical finding (finding) > disease > mental disorder > Developmental mental disorder > Intellectual disability > Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)
... > Clinical finding (finding) > disease > developmental disorder > Neurodevelopmental disorder > Developmental mental disorder > Intellectual disability > Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)

Preferred term

Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)  

Type

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

Associated morphology

Finding site

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/787093004

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