Phenotype #0000257386

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	00361993
Associated disease	MYOP
Diagnosis/Initial	-
Diagnosis/Definite	-
Phenotype details	Hypotonia HP:0001252
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Ibrahim Sahin
Database submission license
Created by	Ibrahim Sahin
Date created	2021-04-13 11:57:54 +02:00 (CEST)
Date last edited	2021-04-14 15:54:24 +02:00 (CEST)

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