Phenotype #0000051922

Individual ID	00072217
Associated disease	?
Diagnosis/Initial	myopathy
Diagnosis/Definite	myopathy, myofibrillar, type 1 (MFM-1)
Phenotype details	Muscular weakness (HP:0001324), complete atrioventricular block (HP:0001678), Pacemaker, elevate serum creatine phosphokinase (HP:0003236),
Inheritance	Familial, autosomal dominant
Age/Examination	39y (39 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
Owner name	Pieter Klap
Database submission license	No license selected
Created by	Pieter Klap
Date created	2016-06-01 10:05:19 +02:00 (CEST)
Date last edited	2017-09-08 13:02:04 +02:00 (CEST)

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