Global Variome shared LOVD

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Phenotype #0000247363 Individual ID 00001467 Associated disease IP Diagnosis/Initial incontinentia pigmenti Diagnosis/Definite IP Inheritance Familial, X-linked recessive Phenotype details see paper; ..., incontinentia pigmenti, osteopetrosis, lymphedema, ectodermal dysplasia, immune deficiency Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license No license selected Created by Johan den Dunnen Date created 2021-02-07 11:56:49 +01:00 (CET) Date last edited 2021-02-07 14:44:37 +01:00 (CET)

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