Phenotype #0000203929

Individual ID 00266150
Associated disease IMD
Phenotype details see paper; …, spastic paraparesis, MRI dorsal spinecord atrophy, MRI brain normal
Diagnosis/Initial hereditary spastic paraplegias
Inheritance Familial, autosomal recessive
Diagnosis/Definite SPG-76
Age/Examination 20y-23y
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-10-15 02:39:58 +02:00 (CEST)
Date last edited 2019-10-15 02:48:38 +02:00 (CEST)

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