Disease #00077 (NPHP11 (nephronophthisis, type 11 (NPHP-11)), OMIM:613550)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NPHP11
Name	nephronophthisis, type 11 (NPHP-11)
OMIM ID	613550
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TMEM67
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-09 15:03:49 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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