Global Variome shared LOVD

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Phenotype #0000229644 Individual ID 00302562 Associated disease PAP Phenotype details see paper; ..., normal psychomotor development; no gelastic epilepsy; no microcephaly; no dysmorphic facial features; no chest and rib abnormalities; postaxial polydactyly; 2/3 syndactyly; cardiac defect; no Hirschsprung disease Diagnosis/Initial postaxial polydactyly Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 8y (8 years) Age/Onset - Phenotype/Onset - Protein - Owner name Sophie Thomas Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2020-05-24 16:50:39 +02:00 (CEST) Date last edited N/A

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