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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