Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000239782 Individual ID 00316036 Associated disease GCCD1 Phenotype details hyperpigmentation Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Familial Glucocorticoid Deficiency Age/Examination 03y (3 years) Age/Diagnosis 03y Age/Onset - Phenotype/Onset - Protein - Owner name Wenjuan Qiu Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Wenjuan Qiu Date created 2020-11-02 09:44:17 +01:00 (CET) Date last edited 2020-11-02 12:47:27 +01:00 (CET)

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