Phenotype #0000060396

Individual ID 00080827
Associated disease CMT-2P
Phenotype details Charcot-Marie-Tooth disease, axonal, type 2P (OMIM:614436)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Daniel Trujillano