Congenital disorder of deglycosylation 2

Preferred Label : Congenital disorder of deglycosylation 2;

Symbol : CDDG2;

Type : Phenotype, molecular basis known;

Prefixed ID : #619775;

Details

Origin ID

619775;

UMLS CUI

C5676931;

Genes related to phenotype
- Mannosidase, alpha, class 2c, member 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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