Global Variome shared LOVD

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

Phenotype #0000129992 Individual ID 00165097 Associated disease SHFYNG Phenotype details see paper; ... Diagnosis/Initial Prader-Willi syndrome-like Inheritance Isolated (sporadic) Diagnosis/Definite SHFYNG Age/Examination 01y (1 year) 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 14:31:08 +02:00 (CEST) Date last edited 2025-10-12 16:53:05 +02:00 (CEST)

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