Phenotype #0000303956

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00411929
Associated disease	myotonia
Phenotype details	myotonia; EMG no myotonia; no muscle weakness; generalized muscle hypertrophy; myopathy not painful; no episodic paralysis
Diagnosis/Initial	non-dystrophic myotonia
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Onset	5y
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2022-06-20 13:19:24 +02:00 (CEST)
Date last edited	N/A

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