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 InternationalCreative Commons License
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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