Phenotype #0000058659

Individual ID 00078903
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details neuropathy, hereditary sensory, with spastic paraplegia; spastic paraplegia, progressive sensory loss, mutilating acropathy involving both upper/lower limbs; MRI severe atrophy spinal cord predominantly posterior tract
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset early infancy
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2012-10-26 11:36:17 +02:00 (CEST)
Date last edited 2012-11-03 11:17:50 +01:00 (CET)

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