Global Variome shared LOVD

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Phenotype #0000279353 Individual ID 00385558 Associated disease - Phenotype details retinitis pigmentosa, postaxial polydactyly, obesity, hypogonadism, AN,FL,MR,PS Diagnosis/Initial Bardet–Biedl syndrome (BBS) Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2021-10-13 10:28:12 +02:00 (CEST) Date last edited N/A

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