Phenotype #0000041867

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00055212
Associated disease	LMPHM1
Phenotype details	Milroy Disease; Typical Milroy Disease with positive family history (father and cousin are mutation positive).
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Michel van Geel
Database submission license
Created by	Michel van Geel
Date created	2011-10-21 19:42:08 +02:00 (CEST)
Date last edited	2012-07-13 16:23:23 +02:00 (CEST)

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