Phenotype #0000043145

Individual ID 00056457
Associated disease CMT2F
Phenotype details progressive symmetrical weakness, atrophy distal limb muscles initially involving legs particularly peroneal muscles, depressed or absent tendon reflexes, mild/moderate distal
sensory abnormalities; age onset 15–25y
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-11-05 16:10:33 +01:00 (CET)
Date last edited 2016-01-11 07:37:19 +01:00 (CET)

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