Global Variome shared LOVD

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Phenotype #0000288571 Individual ID 00395371 Associated disease FOP Phenotype details see paper; ..., typical great toe malformation, knee osteochondroma; 5y-ectopic ossification unclear, 7 lesions; no deafness; low IQ, bald Diagnosis/Initial classic fibrodysplasia ossificans progressiva Inheritance Unknown Diagnosis/Definite FOP Age/Examination 52y (52 years) Age/Diagnosis 2y 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 12:53:42 +01:00 (CET) Date last edited N/A

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