Global Variome shared LOVD

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Phenotype #0000273616 Individual ID 00379762 Associated disease RDCCAS Phenotype details HP:0001123, HP:0000639, HP:0030515, HP:0000480 Diagnosis/Initial Phenotype information related to dystrophy, retinal, iris coloboma, and comedogenic acne syndrome (RDCCAS) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jinu Han Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Jinu Han Date created 2021-08-09 06:29:26 +02:00 (CEST) Date last edited 2021-08-11 14:36:30 +02:00 (CEST)

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