Phenotype #0000186537

Individual ID 00246693
Associated disease SPG
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Maartje Pennings
Database submission license No license selected
Created by Maartje Pennings
Date created 2019-07-16 13:35:12 +02:00 (CEST)
Date last edited 2019-07-16 17:46:08 +02:00 (CEST)

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