Phenotype #0000339508

Individual ID 00450448
Associated disease SPG
Phenotype details see paper; ..., myopathy, motor delay, unsteady gait, gowers sign
Diagnosis/Initial spastic paraplegia
Inheritance Familial, autosomal recessive
Diagnosis/Definite SPG89
Age/Examination 6y (6 years)
Age/Diagnosis -
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 2024-05-27 09:25:31 +02:00 (CEST)
Date last edited N/A

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