Phenotype #0000001869

Individual ID 00003018
Associated disease IBMPFD1
Phenotype details hereditary spastic paraplegia
Diagnosis/Initial hereditary spastic paraplegia
Inheritance Isolated (sporadic)
Diagnosis/Definite IBMPFD
Age/Examination -
Age/Diagnosis -
Age/Onset 06y
Phenotype/Onset -
Protein -
Owner name Marcel Nelen
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-10-02 11:35:03 +02:00 (CEST)
Date last edited 2022-11-17 09:49:29 +01:00 (CET)

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