Disease #04189 (NPHPRC (nephronophthisis-related ciliopathy (NPHP-RC)))

Official abbreviation NPHPRC
Name nephronophthisis-related ciliopathy (NPHP-RC)
OMIM ID -
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2015-02-14 16:29:28 +01:00 (CET)
Date last edited 2021-12-11 13:56:28 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00032320 - PubMed: Schueler 2015, Journal: Schueler 2015 patient, unaffected heterozygous carrier parents ? yes United Kingdom (Great Britain) - - - - - NPHPRC see paper; 11m-hepatic fibrosis; 14y-end-stage renal disease (ESRD) from NPHP; ... BIRC6, CCDC66, CLDN16, DCDC2, TATDN3 BIRC6, CCDC66, CLDN16, DCDC2, TATDN3 5 1 Johan den Dunnen
00032321 - PubMed: Schueler 2015, Journal: Schueler 2015 patient, unaffected heterozygous carrier parents - no Czech Republic - - - - - NPHPRC see paper; hepatic fibrosis; 2y-liver transplantation; no retinal degeneration, no cerebellar vermis hypoplasia, no hydrocephalus, no obesity, no bone disease DCDC2 DCDC2 2 1 Johan den Dunnen
00213208 30609407-F1279-21 PubMed: Choi 2019 2-generation family, affected, unaffected heterozygous carrier parents - - - European - - - - NPHPRC increased echogenicity, medullary cysts, proteinuria, cortical deafness, atrial septal defect, growth retardation, short stature, coloboma, aplasia of vermis, corpus callosum hypoplasia; 5y-end-stage renal disease ADAMTS9 ADAMTS9 1 1 Johan den Dunnen
00213209 30609407-FamA5048-21 PubMed: Choi 2019 2-generation family, affected, unaffected heterozygous carrier parents - yes - Arab - - - - NPHPRC NPHP, nonselective proteinuria, end-stage renal disease since infancy, sensorineural deafness, hepatosplenomegaly, short stature, anemia, thrombocytopenia, osteopenia, rickets; 2y-renal biopsy microcystic dilatation of tubules, immature glomeruli ADAMTS9 ADAMTS9 1 1 Johan den Dunnen
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