Disease #04438 (NPHP19 (nephronophthisis, type 19 (NPHP-19)), OMIM:616217)

Official abbreviation NPHP19
Name nephronophthisis, type 19 (NPHP-19)
OMIM ID 616217
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DCDC2
Associated tissues -
Disease features -
Remarks -

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