Phenotype #0000228515

Individual ID 00301247
Associated disease neuropathy
Diagnosis/Initial CMT2 (motor predominant)
Diagnosis/Definite -
Phenotype details moderate severity; axonal motor NCS; sensory NCS upper limbs normal, sensory NCS lower limbs reduced; mild hearing loss
Inheritance Familial, autosomal recessive
Age/Examination 60y (60 years)
Age/Onset 15y
Phenotype/Onset falls
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

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.