MCID: ATS245
MIFTS: 4

Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency

Categories: Blood diseases, Rare diseases

Aliases & Classifications for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2...

MalaCards integrated aliases for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency:

Name: Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency 60

Characteristics:

Orphanet epidemiological data:

60
autosomal recessive severe congenital neutropenia due to cxcr2 deficiency
Inheritance: Autosomal recessive; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:

Orphanet: 60  
Rare immunological diseases


External Ids:

ICD10 via Orphanet 35 D70
Orphanet 60 ORPHA420699

Summaries for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2...

MalaCards based summary : Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency An important gene associated with Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2 Deficiency is CXCR2 (C-X-C Motif Chemokine Receptor 2).

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Sources for Autosomal Recessive Severe Congenital Neutropenia Due to Cxcr2...

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