Phenotype #0000292582

Individual ID 00399477
Associated disease CMTX1
Phenotype details see paper;…, decreased compound muscle action potential amplitude (HP:0033383)
Diagnosis/Initial -
Inheritance Familial, X-linked dominant
Diagnosis/Definite CMT1X
Age/Examination 41y (41 years)
Age/Diagnosis 41y
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Maeve Soen
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maeve Soen
Date created 2022-01-20 22:13:34 +01:00 (CET)
Date last edited 2022-01-24 11:47:42 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.