Phenotype #0000161684

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00213209
Associated disease	NPHPRC
Phenotype details	NPHP, nonselective proteinuria, end-stage renal disease since infancy, sensorineural deafness, hepatosplenomegaly, short stature, anemia, thrombocytopenia, osteopenia, rickets; 2y-renal biopsy microcystic dilatation of tubules, immature glomeruli
Diagnosis/Initial	nephronophthisis
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2019-01-12 11:36:18 +01:00 (CET)
Date last edited	N/A

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