Phenotype #0000291859

Individual ID 00398775
Associated disease CMTDIB;CMT2M
Phenotype details Peripheral neuropathy (HP:0009830), Decreased nerve conduction velocity (HP:0000762)
Diagnosis/Initial CMT
Inheritance Unknown
Diagnosis/Definite -
Age/Examination 67y (67 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Yvet den Hartog
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Yvet den Hartog
Date created 2022-01-12 13:00:00 +01:00 (CET)
Date last edited 2022-01-18 16:21:19 +01:00 (CET)

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