Phenotype #0000042440

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	00055785
Associated disease	LMPHM1
Phenotype details	Milroy Disease; Congenital lymphoedema of both feet.
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	0d
Phenotype/Onset	-
Protein	-
Owner name	Pia Ostergaard
Database submission license	No license selected
Created by	Pia Ostergaard
Date created	2012-09-13 10:14:58 +02:00 (CEST)
Date last edited	N/A

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