Global Variome shared LOVD

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Phenotype #0000269368 Individual ID 00374158 Associated disease GCPS Phenotype details hand bilateral postaxial polydactyly; feet bilateral preaxial polydactyly; syndactyly; macrocephaly; no widely spaced eyes; no developmental delay Diagnosis/Initial Greig cephalopolysyndactyly syndrome Inheritance Familial, autosomal dominant Diagnosis/Definite GCPS Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-05-24 10:55:07 +02:00 (CEST) Date last edited N/A

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