Phenotype #0000187182

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00248174
Associated disease	HCINF2
Phenotype details	Nephrocalcinosis, Muscular hypotonia, Failure to thrive
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Valeriia Apukhtina
Database submission license	No license selected
Created by	Valeriia Apukhtina
Date created	2019-07-19 15:31:54 +02:00 (CEST)
Date last edited	2019-07-22 15:50:05 +02:00 (CEST)

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