Global Variome shared LOVD

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Phenotype #0000276987 Individual ID 00383200 Associated disease - Phenotype details retinitis pigmentosa, obesity, polydactyly, mental retardation, renal disease, developmental delaySeizures Diagnosis/Initial Bardet–Biedl Syndrome (BBS) Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 9y (9 years) 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 2021-09-28 01:33:29 +02:00 (CEST) Date last edited N/A

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