Global Variome shared LOVD

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Phenotype #0000351722 Individual ID 00466358 Associated disease CMH11 Phenotype details Arthrogryposis multiplex congenita Distal amyotrophy Fatigable weakness Camptodactyly of 2nd-5th fingers Diagnosis/Initial Congenital myopathy Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Camille Verebi Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Camille Verebi Date created 2025-08-22 17:26:47 +02:00 (CEST) Date last edited 2025-08-25 15:34:04 +02:00 (CEST)

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