Global Variome shared LOVD

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Phenotype #0000042472 Individual ID 00055817 Associated disease LMPHM1 Phenotype details Milroy Disease; Congenital bilateral lymphoedema of the feet. One episode of cellulitis. Family history: father had bilateral lymphoedema of the feet. Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis 0d Age/Onset 0d Phenotype/Onset - Protein - Owner name Pia Ostergaard Database submission license No license selected Created by Pia Ostergaard Date created 2012-09-14 18:14:38 +02:00 (CEST) Date last edited N/A

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