Phenotype #0000167555

Individual ID 00218998
Associated disease CMT
Phenotype details CMT-DIE; no family history; typical phenotype with CMT and focal segmental
glomerulosclerosis
Diagnosis/Initial Charcot-Marie-Tooth diseae
Inheritance Unknown
Diagnosis/Definite CMTDIE
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
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 2019-02-05 12:23:36 +01:00 (CET)
Date last edited 2019-02-05 16:43:59 +01:00 (CET)

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