Disease #00074 (NPHS1 (nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF))), OMIM:256300)

Official abbreviation NPHS1
Name nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF))
OMIM ID 256300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene NPHS1
Associated tissues -
Disease features -
Remarks -
Date created 2012-11-09 14:39:22 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00017906 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS1 - NPHS1 NPHS1 2 1 Elisabet Ars Criach
00017907 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS1 - NPHS1 NPHS1 1 1 Elisabet Ars Criach
00019917 - PubMed: Bullich 2015, Journal: Bullich 2015 - - - Spain - - - - - NPHS1 - NPHS1 NPHS1 1 1 Elisabet Ars Criach
00306210 109 - - M - China - - - - - NPHS1 - NPHS1 NPHS1 1 1 Sha Hong
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