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X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Chronic granulomatous disease
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Neutrophil immunodeficiency syndrome
Synonym(s):
- X-linked MSMD due to CYBB deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CYBB P04839300481
No signs/symptoms info available.