Global Variome shared LOVD

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Phenotype #0000036660 Individual ID 00049885 Associated disease RTS2 Inheritance Familial, autosomal recessive Diagnosis/Initial - Age/Examination 11y (11 years) Diagnosis/Definite - Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details alopecia, dystrophic nails, osteopenia, short stature, gastrointestinal symptoms during infancy Protein - Owner name Sabina Gallati, Prof. Database submission license No license selected Created by Sabina Gallati, Prof. Date created 2015-09-13 23:09:10 +02:00 (CEST) Date last edited 2016-01-26 02:58:19 +01:00 (CET)

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