Phenotype #0000042468

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00055813
Associated disease	LMPHM1
Phenotype details	Milroy Disease; Congenital lower limb lymphoedema, learning difficulties and behavioural problems.
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Pia Ostergaard
Database submission license	No license selected
Created by	Pia Ostergaard
Date created	2012-09-14 18:03:32 +02:00 (CEST)
Date last edited	N/A

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