Global Variome shared LOVD

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Phenotype #0000232934 Individual ID 00307129 Associated disease CMT2P Phenotype details Weakness of foot dorsiflexion and lowering since the 30th year of life, distally emphasized sensorimotor axonal PNP. FA: Brother of the father also PNP since 70th year, father died with 29 years without symptoms of PNP, daughter also affected (known since 28th year) Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset 30y Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2020-08-03 16:49:41 +02:00 (CEST) Date last edited 2020-08-04 21:44:30 +02:00 (CEST)

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