Global Variome shared LOVD

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Phenotype #0000326917 Individual ID 00436835 Associated disease OBAIRH Phenotype details see paper; ..., obesity, adrenal insufficiency, red hair syndrome Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite OBAIRH 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 2023-10-10 21:26:59 +02:00 (CEST) Date last edited N/A

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