Disease #00375 (NPHP13 (nephronophthisis, type 13 (NPHP-13)), OMIM:614377)

Official abbreviation NPHP13
Name nephronophthisis, type 13 (NPHP-13)
OMIM ID 614377
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene WDR19
Associated tissues -
Disease features -
Remarks -
Date created 2014-05-02 09:58:44 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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