Phenotype #0000297648

Individual ID 00405095
Associated disease CMT
Phenotype details 36-y male with progressive weakness and wasting of both upper and lower limbs
Diagnosis/Initial CMT1F
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 32y (32 years)
Age/Diagnosis -
Age/Onset 17y
Phenotype/Onset -
Protein -
Owner name Sherifa Ahmed Hamed
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Sherifa Ahmed Hamed
Date created 2022-03-16 00:09:44 +01:00 (CET)
Date last edited 2022-03-17 09:22:39 +01:00 (CET)

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