Phenotype #0000227538

Individual ID 00300236
Associated disease NLS2
Phenotype details HP:0001558, HP:0001511, HP:0000340, HP:0000470, HP:0000377, HP:0000369, HP:0000153, HP:0012472, HP:0000347, HP:0007651, HP:0000252, HP:0001371, HP:0006101, HP:0001770, HP:0001838, HP:0001762, HP:0008064,HP:0000951, HP:0002089
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein p.(Ala99Val)
Owner name Fatima Abdelfattah
Database submission license No license selected
Created by Fatima Abdelfattah
Date created 2020-04-24 14:36:33 +02:00 (CEST)
Date last edited 2020-04-26 11:05:04 +02:00 (CEST)

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