Phenotype #0000015252

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00016850
Associated disease	MYMY6
Phenotype details	0m: Achalasia; (Mallignant)Hypertension, Raynaud phenomenon, Abnormal Platelet-aggregation, erectile dysfunction since adolescence
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	30y (30 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Marianne Vos (LOVD-team)
Database submission license	No license selected
Created by	Marianne Vos (LOVD-team)
Date created	2014-06-03 14:02:03 +02:00 (CEST)
Date last edited	2016-06-18 22:24:58 +02:00 (CEST)

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