Phenotype #0000084301

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00106497
Associated disease	MFM
Phenotype details	Patients described to have features of myofibrillar myopathy pathologically, no nemaline bodies seen.
Diagnosis/Initial	-
Inheritance	Unknown
Diagnosis/Definite	-
Age/Examination	-
Age/Onset	1d
Phenotype/Onset	-
Protein	-
Owner name	Kristen Nowak
Database submission license	No license selected
Created by	Kristen Nowak
Date created	2015-01-09 04:41:39 +01:00 (CET)
Date last edited	N/A

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