Phenotype #0000291834

Individual ID 00398668
Associated disease SPG10
Phenotype details Peripheral neuropathy (HP:0009830), Spastic paraplegia (HP:0001258), No decreased nerve conduction velocity (-HP:0000762)
Diagnosis/Initial CMT
Inheritance Familial, autosomal dominant
Diagnosis/Definite SPG10
Age/Examination 60y (60 years)
Age/Diagnosis -
Age/Onset 40y
Phenotype/Onset Peripheral neuropathy (HP:0009830), Spastic paraplegia (HP:0001258), No decreased nerve conduction velocity (-HP:0000762)
Protein -
Owner name Yvet den Hartog
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Yvet den Hartog
Date created 2022-01-11 15:01:03 +01:00 (CET)
Date last edited 2022-01-18 16:06:59 +01:00 (CET)

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