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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
autosomal dominant severe congenital neutropenia +   
Severe Congenital Neutropenia 10  
Infantile onset of neutropenia, which may be associated with bacterial infections, including skin abscesses. Caused by compound heterozygous mutation in the SRP68 gene on chromosome 17q25.
severe congenital neutropenia 3  
severe congenital neutropenia 4 +   
severe congenital neutropenia 5  
severe congenital neutropenia 6  
severe congenital neutropenia 7  
X-linked severe congenital neutropenia  

Synonyms
Exact Synonyms: Neutropenia, severe congenital, 10, autosomal recessive ;   SCN10
Primary IDs: OMIM:620534

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