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Congenital Nephrotic Syndrome, Finnish Type (MONDO:0009732)

Congenital nephrotic syndrome, Finnish type is characterized by protein loss beginning during fetal life.

Overview

Category

Ontology ID

Internal:10944

Synonyms

Finnish congenital nephrosis

congenital nephrotic syndrome - Finnish type

congenital nephrotic syndrome, Finnish type

nephrotic syndrome - NPHS1 associated

CnF

NPHS1

congenital nephrotic syndrome 1

congenital nephrotic syndrome Finnish type

nephrosis 1, congenital, Finnish type

nephrosis, congenital

nephrotic syndrome, congenital

nephrotic syndrome, type 1

Mapped terms

DOID:0080390

GARD:0001500

MEDGEN:98011

MedDRA:10060740

NANDO:2200110

NCIT:C122795

OMIM:256300

Orphanet:839

SCTID:197601003

UMLS:C0403399

Child terms

Unknown children.