Global Variome shared LOVD

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Phenotype #0000129914 Individual ID 00165041 Associated disease MSSD Phenotype details syndactyly, polydactyly, phalangeal reduction and hypoplastic nails,camptodactyly with hypoplastic nails, bilateral mesoaxial synostotic syndactyly, and postaxial polydactyly in the right hand Diagnosis/Initial Mesoaxial synostotic syndactyly Inheritance Familial, autosomal recessive Diagnosis/Definite Mesoaxial synostotic syndactyly Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Muhammad Umair Database submission license No license selected Created by Muhammad Umair Date created 2018-06-21 06:56:27 +02:00 (CEST) Date last edited 2018-06-21 12:19:18 +02:00 (CEST)

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