Disease #02506 (NPHP3 (nephronophthisis, type 3 (NPHP-3)), OMIM:604387)

Official abbreviation NPHP3
Name nephronophthisis, type 3 (NPHP-3)
OMIM ID 604387
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene NPHP3
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

3 entries on 1 page. Showing entries 1 - 3.
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00164068 Sayer JA - - F no United Kingdom (Great Britain) - - - - - NPHP3 congenital hepatic fibrosis end stage renal disease NPHP3 NPHP3 2 1 John Sayer
00164069 Sayer JA - - ? no Germany - - - - - NPHP3 Severe chronic tubule-interstitial damage with atrophy of tubules, interstitial fibrosis and moderate interstitial inflammation Hypertension End stage renal disease 15 years NPHP3 NPHP3 2 1 John Sayer
00164805 CW - - F no United Kingdom (Great Britain) - - - - - NPHP3 congenital hepatic fibrosis end stage renal disease NPHP3 NPHP3 2 1 John Sayer
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