Disease #00252 (proteinuria, hypercalciuria, nephrocalcinosis, OMIM:308990)

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Official abbreviation	-
Name	proteinuria, hypercalciuria, nephrocalcinosis
OMIM ID	308990
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CLCN5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-20 13:44:39 +02:00 (CEST)
Date last edited	N/A