Phenotype #0000232937

Individual ID 00307132
Associated disease CMT-2P
Phenotype details Hereditary polyneuropathy, sensorimotor primary axonal PNP (sensory > motor), father also affected
Diagnosis/Initial 58y
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner