Disease #03270 (NPHPL1 (nephronophthisis-like nephropathy, type 1 (NPHPL-1)), OMIM:613159)

Official abbreviation NPHPL1
Name nephronophthisis-like nephropathy, type 1 (NPHPL-1)
OMIM ID 613159
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene XPNPEP3
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)


Individuals

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00472200 - Verebi et al. (submitted) - M - France - - - - - NPHPL1 Exercise-induced rhabdomyolysis * Abnormal mitochondrial morphology * Focal hyperintensity of cerebral white matter on MRI - XPNPEP3 1 1 Camille Verebi
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