Phenotype #0000227533

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00300231
Associated disease	NLS2
Phenotype details	HP:0000767
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	p.(Arg61Trp), p.(Ala99Val)
Owner name	Fatima Abdelfattah
Database submission license	No license selected
Created by	Fatima Abdelfattah
Date created	2020-04-24 13:02:31 +02:00 (CEST)
Date last edited	2020-04-26 11:02:54 +02:00 (CEST)

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