Global Variome shared LOVD

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Phenotype #0000288582 Individual ID 00395382 Associated disease FOP Phenotype details 10y-heterotopic ossification; no great toe malformation, progressive heterotopic ossification, sparse thin scalp hair, no heterochromia, no mitral valve prolapse Diagnosis/Initial variant fibrodysplasia ossificans progressiva Inheritance Isolated (sporadic) Diagnosis/Definite FOP Age/Examination 25y (25 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 13:07:09 +01:00 (CET) Date last edited N/A

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