Phenotype #0000228502

Individual ID 00301234
Associated disease neuropathy
Diagnosis/Initial dHMN
Diagnosis/Definite -
Phenotype details mild severity; axonal motor NCS; sensory NCS upper limbs normal, sensory NCS lower limbs normal
Inheritance Familial, autosomal recessive
Age/Examination 31y (31 years)
Age/Onset 15y
Phenotype/Onset distal atrophy of lower limbs
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 2020-05-10 11:49:06 +02:00 (CEST)
Date last edited N/A

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