Global Variome shared LOVD

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Phenotype #0000282073 Individual ID 00388532 Associated disease - Phenotype details intellectual disability, obesity, polydactyly, renal fibrosis, BMI: nd, speech delay or disorder, development delay, dental crowding, behavioral problems Diagnosis/Initial Bardet-Biedl syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite Bardet-Biedl syndrome Age/Examination 10y (10 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-11-04 13:39:46 +01:00 (CET) Date last edited N/A

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