Phenotype #0000129995

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00165099
Associated disease	SHFYNG
Phenotype details	see paper; ...
Diagnosis/Initial	Prader-Willi syndrome-like
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	SHFYNG
Age/Examination	23y05m (23 years, 5 months)
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 14:44:39 +02:00 (CEST)
Date last edited	2025-10-12 16:58:23 +02:00 (CEST)

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