Neutropenia, severe congenital, 9, autosomal dominant

Preferred Label : Neutropenia, severe congenital, 9, autosomal dominant;

Symbol : SCN9;

Type : Phenotype, molecular basis known;

Prefixed ID : #619813;

Details

Origin ID

619813;

UMLS CUI

C5676954;

Genes related to phenotype
- Caseinolytic peptidase b [OMIM gene]
ORDO concept(s)
- Autosomal dominant severe congenital neutropenia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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