Phenotype #0000227023

Individual ID	00295971
Associated disease	NLS2
Phenotype details	HP:0001511, HP:0001558, HP:0000340, HP:0000470, HP:0000377, HP:0000369,HP:0012472, HP:0000153, HP:0000218, HP:0000347, HP:0000316, HP:0000518, HP:0000482, HP:000252, HP:0002536, HP:0012639, HP:0001274, HP:0001371, HP:0001838, HP:0012210, HP:0000924, HP:0001627, HP:0008064
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 15:47:53 +02:00 (CEST)
Date last edited	2020-04-21 10:02:34 +02:00 (CEST)

Global Variome shared LOVD