Disease #03447 (NPHP12;JBTS11 (nephronophthisis, type 12 (NPHP-12, Joubert syndrome 11 (JBTS-11))), OMIM:613820)

Official abbreviation	NPHP12;JBTS11
Name	nephronophthisis, type 12 (NPHP-12, Joubert syndrome 11 (JBTS-11))
OMIM ID	613820
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TTC21B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD