Global Variome shared LOVD

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Phenotype #0000042424 Individual ID 00055769 Associated disease LMPHM1 Phenotype details Milroy Disease; Typical Milroy disease with positive family history. Father (mutation positive) and two sons are affected. 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 2012-07-13 15:18:22 +02:00 (CEST) Date last edited N/A

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