Global Variome shared LOVD
CLCN7 (chloride channel, voltage-sensitive 7)
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Phenotype #0000172772
Individual ID
00228956
Associated disease
pyr.kin. deficiency
Phenotype details
hemolytic anemia
Diagnosis/Initial
-
Inheritance
Unknown
Diagnosis/Definite
-
Age/Examination
-
Age/Diagnosis
-
Age/Onset
-
Phenotype/Onset
-
Protein
-
Owner name
Richard van Wijk
Database submission
license
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International
Created by
Richard van Wijk
Date created
2011-11-20 12:53:49 +01:00 (CET)
Date last edited
2022-02-18 22:20:21 +01:00 (CET)
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