Global Variome shared LOVD

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

Phenotype #0000129993 Individual ID 00165100 Associated disease SHFYNG Phenotype details see paper; ... Diagnosis/Initial Prader-Willi syndrome-like Inheritance Familial, autosomal dominant Diagnosis/Definite SHFYNG Age/Examination 12y (12 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Yutak Negishi Database submission license No license selected Created by Yutak Negishi Date created 2018-06-25 14:41:32 +02:00 (CEST) Date last edited 2025-10-12 17:00:23 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.