Global Variome shared LOVD

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Phenotype #0000130105 Individual ID 00165098 Associated disease SHFYNG Phenotype details see paper; ... Diagnosis/Initial Prader-Willi syndrome-like Inheritance Isolated (sporadic) Diagnosis/Definite SHFYNG Age/Examination 06y03m (6 years, 3 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Yutak Negishi Database submission license No license selected Created by Johan den Dunnen Date created 2018-07-02 15:00:31 +02:00 (CEST) Date last edited 2025-10-12 16:56:03 +02:00 (CEST)

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