Phenotype #0000254612

Individual ID 00359316
Associated disease HMN
Phenotype details see paper; ..., distal weakness LL+UL; no proximal weakness; sensory involvement LL; pes cavus; no CNS involvement; feet paresthesia
Diagnosis/Initial distal hereditary motor neuropathy
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 15y (15 years)
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 2021-03-19 08:49:14 +01:00 (CET)
Date last edited N/A

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