Phenotype #0000141810

Individual ID 00176991
Associated disease SPG
Phenotype details Gait difficulties, spastic paraplegia
Diagnosis/Initial Spastic paraplegia
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 28y
Phenotype/Onset -
Protein -
Owner name Inge Meijer
Database submission license No license selected
Created by Inge Meijer
Date created 2018-08-14 21:11:19 +02:00 (CEST)
Date last edited N/A

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