Phenotype #0000044577

Individual ID 00004160
Associated disease RTS2
Inheritance Familial, autosomal recessive
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details see paper; two siblings with a mild phenotype, mainly restricted to the skin, ...
Protein -
Owner name Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
Date created 2016-01-26 03:09:38 +01:00 (CET)
Date last edited 2016-01-26 03:20:21 +01:00 (CET)

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