Granulomatous Disease, Chronic, Autosomal Recessive, 3 (CGD3)

Alias:
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type 3
Autosomal Recessive Chronic Granulomatous Disease Cytochrome B-Positive Type Iii
Cgd3
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Iii
Granulomatous Disease, Chronic, Autosomal Recessive Cytochrome B-Positive, Type 3
Chronic Granulomatous Disease Autosomal Recessive Cytochrome B-Positive Type Iii
Cgd, Autosomal Recessive Cytochrome B-Positive, Type Iii
Granulomatous Disease, Chronic, Due to Ncf4 Deficiency
Autosomal Recessive Cytochrome B-Positive Cgd Type Iii
Cgd Autosomal Recessive Cytochrome B-Positive Type Iii
Chronic Granulomatous Disease 3, Autosomal Recessive
Chronic Granulomatous Disease Due to Ncf4 Deficiency
Granulomatous Disease Chronic Due to Ncf4 Deficiency
Autosomal Recessive Chronic Granulomatous Disease 3
Cdg3
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Granulomatous Disease, Chronic, Autosomal Recessive, 3, also known as granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3, is related to lung abscess and granulomatous disease, chronic, autosomal recessive, 1. An important gene associated with Granulomatous Disease, Chronic, Autosomal Recessive, 3 is NCF4 (Neutrophil Cytosolic Factor 4), and among its related pathways/superpathways are CXCR4-mediated signaling events and Detoxification of Reactive Oxygen Species. Affiliated tissues include skin and lung, and related phenotypes are abdominal pain and diarrhea
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
12
54
7

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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