Global Variome shared LOVD

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Phenotype #0000042437 Individual ID 00055782 Associated disease LMPHM1 Phenotype details Milroy Disease; Congenital right foot lymphoedema. Left foot swelling developed within two years. Upslanting toenails and prominent large calibre veins present. FHx: mother and maternal grandmother had childhood onset congenital lymphoedema of the feet. 2 affected sisters (one has a son with a hydrocele). Patients son also has a hydrocele. 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 09:42:58 +02:00 (CEST) Date last edited 2012-09-13 09:47:44 +02:00 (CEST)

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