Global Variome shared LOVD
CNKSR1 (connector enhancer of kinase suppressor of ...)
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Global Variome, with Curator vacancy
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Phenotype #0000354900
Individual ID
00469755
Associated disease
skeletal dysplasia
Diagnosis/Initial
skeletal dysplasia
Diagnosis/Definite
ACH
Phenotype details
-
Inheritance
Isolated (sporadic)
Age/Examination
-
Age/Diagnosis
-
Age/Onset
-
Phenotype/Onset
-
Protein
-
Owner name
Johan den Dunnen
Database submission
license
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International
Created by
Johan den Dunnen
Date created
2025-11-20 12:33:13 +01:00 (CET)
Date last edited
N/A
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