Phenotype #0000172766

Individual ID 00229228
Associated disease pyr.kin. deficiency
Phenotype details severe
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Richard van Wijk
Database submission license No license selected
Created by Richard van Wijk
Date created 2012-12-18 15:11:13 +01:00 (CET)
Date last edited 2022-02-18 21:46:50 +01:00 (CET)

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