Global Variome shared LOVD

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Phenotype #0000152820 Individual ID 00204352 Associated disease FOP Phenotype details FOP-plus or FOP variants (variation fron the classic FOP features as defined in PMID19085907 Kaplan FS, et al., 2009); reduction malformation of the digits; mild cognitive impairment Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution-ShareAlike 4.0 International Created by LOVD Date created 2013-04-10 11:05:38 +02:00 (CEST) Date last edited 2013-04-10 11:20:05 +02:00 (CEST)

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