Neutropenia, Severe Congenital, 7, Autosomal Recessive (SCN7)

Alias:
Scn7
Autosomal Recessive Severe Congenital Neutropenia Due to Csf3r Deficiency
Neutropenia, Severe Congenital 7, Autosomal Recessive
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Neutropenia, Severe Congenital, 7, Autosomal Recessive, also known as scn7, is related to severe congenital neutropenia 7. An important gene associated with Neutropenia, Severe Congenital, 7, Autosomal Recessive is CSF3R (Colony Stimulating Factor 3 Receptor). Affiliated tissues include bone marrow and neutrophil, and related phenotypes are neutropenia and recurrent infections
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
10
19

Medical Symptom

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Categorization
Description
HPO Frequency
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No data available

Gene & Mutation

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No data available

Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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