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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