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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome

Preferred term

Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome  

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

Associated morphology

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Is a

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/1179408008

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