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C7

complement C7

HCNC Approved Symbol
C7 (HGNC:1346)
Genomic Coordinates
5:40,909,497 - 40,984,643 (5p13.1)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the C7 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Infections, recurrent
 1 (100.0%)
Meningitis, recurrent
 1 (100.0%)
Recurrent otitis media
 1 (100.0%)
C7 - Gene browser | 3billion