Global Variome shared LOVD

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Phenotype #0000288532 Individual ID 00395332 Associated disease FOP Phenotype details see paper; ..., heterotopic ossification, no malformation great toes, normal development from birth; 17y-heterotopic ossification lumbar area; delayed onset, slower and mild clinical course, little finger camptodactyly Diagnosis/Initial variant fibrodysplasia ossificans progressiva Inheritance Unknown Diagnosis/Definite FOP Age/Examination 22y (22 years) 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 2021-12-05 11:04:18 +01:00 (CET) Date last edited N/A

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