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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Recessive hereditary disorder, NOS > Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1

Preferred term

Carbohydrate deficient glycoprotein syndrome type 2 due to deficiency of mannosidase alpha class 1B member 1  

Type

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

Occurrence

URI

http://www.irandoc.acir/onto/irandoc/733450008

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