Global Variome shared LOVD

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Phenotype #0000210664 Individual ID 00269286 Associated disease obesity Phenotype details postaxial polydactyly, retinal dystrophy, and childhood obesity, no renal problems and developmental delay or intellectual disability. Diagnosis/Initial Initial diagnosis Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 11y (11 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Elles Boon Database submission license No license selected Created by Elles Boon Date created 2020-01-24 15:47:22 +01:00 (CET) Date last edited 2020-05-26 13:00:30 +02:00 (CEST)

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