Global Variome shared LOVD

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Phenotype #0000279748 Individual ID 00385947 Associated disease - Phenotype details obesity, cataract, night blindness, strabismus, Moderate learning disability, polydactyly hand, polydactyly feet, speech disorder, Behavioral-problem, developmental-delay, dental-anomaly, Hirschprung-syndrome 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 2021-10-19 12:24:34 +02:00 (CEST) Date last edited N/A

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