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C176827Level 10

Severe Congenital Neutropenia Type 1, Autosomal Dominant

**Semantic type:** Disease or Syndrome

**Definition:** Severe congenital neutropenia inherited in an autosomal dominant pattern and caused by mutation(s) in the ELANE gene, encoding neutrophil elastase

**Synonyms:** - Neutropenia, Severe Congenital, 1, Autosomal Dominant - SCN1 - Severe Congenital neutropenia (SCN) 1 - Includes cyclic neutropenia

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