Phenotype #0000303463

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00411423
Associated disease	HP1
Phenotype details	-
Diagnosis/Initial	oxalosis
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	Primary hyperoxaluria
Age/Examination	12y (12 years)
Age/Diagnosis	12y
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Aiysha Abid
Database submission license
Created by	Aiysha Abid
Date created	2022-06-13 12:56:12 +02:00 (CEST)
Date last edited	2022-06-17 10:37:07 +02:00 (CEST)

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