Phenotype #0000278766

Individual ID 00384981
Associated disease SPG4
Phenotype details spastic paraplegia
Diagnosis/Initial spastic paraplegia
Inheritance Familial, autosomal dominant
Diagnosis/Definite SPG4
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Julia Mela
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Julia Mela
Date created 2021-10-06 15:47:15 +02:00 (CEST)
Date last edited 2021-10-07 09:10:11 +02:00 (CEST)

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