Disease #05448 (NPHS13 (nephrotic syndrome, type 13 (NPHS-13)), OMIM:616893)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NPHS13
Name	nephrotic syndrome, type 13 (NPHS-13)
OMIM ID	616893
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NUP205
Associated tissues	-
Disease features	autosomal recessive?
Remarks	-
Date created	2018-06-29 10:32:00 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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