Phenotype #0000171330

Individual ID 00183396
Associated disease SPG
Phenotype details onset juvenile, hyposthenia, fatigue, proximal muscle weakness lower limbs, normal CPK, EMG mixed
Diagnosis/Initial spastic paraplegia
Inheritance Familial, autosomal dominant
Diagnosis/Definite SPG-4
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset hyposthenia, fatigue
Protein -
Owner name Johan den Dunnen
Database submission license No license selected
Created by Johan den Dunnen
Date created 2019-03-02 17:25:27 +01:00 (CET)
Date last edited N/A

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