Phenotype #0000228477

Individual ID 00301209
Associated disease neuropathy
Diagnosis/Initial CMT2
Diagnosis/Definite -
Phenotype details mild severity; axonal motor NCS
Inheritance Familial, autosomal recessive
Age/Examination 38y (38 years)
Age/Onset 10y
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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