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 -

  Powered by LOVD v.3.0 Build 29
LOVD software ©2004-2023 Leiden University Medical Center 		There are currently no updates.