Disease #00074

Official abbreviation NPHS-1
Name nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF))
OMIM ID 256300
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene NPHS1
Associated tissues -
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00017906 - - - - - - - - 0 - - NPHS-1 NPHS1 NPHS1 2 1 Elisabet Ars Criach
00017907 - - - - - - - - 0 - - NPHS-1 NPHS1 NPHS1 1 1 Elisabet Ars Criach
00019917 - - - - - - - - 0 - - NPHS-1 NPHS1 NPHS1 1 1 Elisabet Ars Criach
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