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C176602Level 10

Severe Congenital Neutropenia Type 6, Autosomal Recessive

**Semantic type:** Disease or Syndrome

**Definition:** Severe congenital neutropenia inherited in an autosomal recessive pattern and caused by mutation(s) in the JAGN1 gene, encoding protein jagunal homolog 1.

**Synonyms:** - Neutropenia, Severe Congenital, 6, Autosomal Recessive - SCN 6-Autosomal Recessive - SCN6

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