Phenotype #0000227013

Individual ID 00295966
Associated disease NLS1
Phenotype details HP:0001371
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Fatima Abdelfattah
Database submission license No license selected
Created by Fatima Abdelfattah
Date created 2020-04-20 13:18:21 +02:00 (CEST)
Date last edited 2020-04-20 13:24:26 +02:00 (CEST)

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