Global Variome shared LOVD

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Phenotype #0000306966 Individual ID 00415165 Associated disease DKC Inheritance Familial, autosomal recessive Diagnosis/Initial dyskeratosis congenita Age/Examination 25y (25 years) Diagnosis/Definite - Age/Diagnosis - Age/Onset - Phenotype/Onset - Phenotype details abnormalities in skin pigmentation; nail dystrophy; leukoplakia; hair loss, thin eye lashes; no hematological abnormalities Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2022-08-08 19:48:19 +02:00 (CEST) Date last edited N/A

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