nephrosis, congenital

Preferred Label : nephrosis, congenital;

MeSH hyponym : Nephrotic Syndrome, Idiopathic; Nephrotic Syndrome, Early-Onset, Type 3; Nphs3; Nephrosis 1, congenital, Finnish type; Finnish congenital nephrosis; Congenital nephrotic syndrome, Finnish type; Congenital nephrotic syndrome 1;

Details

Origin ID

C535761;

UMLS CUI

C3501848;

Automatic exact mappings (from CISMeF team)
- Idiopathic Nephrotic Syndrome [NCIt concept]
- Idiopathic nephrotic syndrome [ORDO Disease]
- Idiopathic nephrotic syndrome [HPO term]
- Minimal change disease (disorder) [SNOMED CT concept]
- Nephrotic syndrome [ICD-10 category (who)]
- Nephrotic syndrome [ICD-10 category]
- Nephrotic syndrome, type 2 [OMIM Phenotype]
- Nephrotic syndrome, type 3 [OMIM Phenotype]
- PLCE1 wt Allele [NCIt concept]
- nephrotic syndrome type 2 [DO Concept]
- nephrotic syndrome type 3 [DO Concept]
- phospholipase C epsilon 1 [ORDO Gene]
Currated CISMeF NLP mapping
- Congenital Nephrotic Syndrome [NCIt concept]
- Congenital nephrotic syndrome [MedDRA Preferred Term]
- Congenital nephrotic syndrome [HPO term]
- Congenital nephrotic syndrome (disorder) [SNOMED CT concept]
- Congenital nephrotic syndrome - finnish type [MedDRA LLT]
- Familial nephrotic syndrome [MedDRA LLT]
- Finnish congenital nephrotic syndrome (disorder) [SNOMED CT concept]
- Nephrotic Syndrome - NPHS1 Associated [NCIt concept]
- Nephrotic syndrome, type 1 [OMIM Phenotype]
- congenital nephrotic syndrome [SNOMED Notion]
- congenital nephrotic syndrome [Disease (Nov.)]
- familial nephrotic syndrome [DO Concept]
- nephrotic syndrome type 1 [Disease (Nov.)]
DO Cross reference
- familial nephrotic syndrome [DO Concept]
HPO term
- Congenital nephrotic syndrome [HPO term]
MeSH term(s) associated for indexing
- nephrotic syndrome [MeSH Descriptor]
ORDO relation(s)
- Congenital nephrotic syndrome, Finnish type [ORDO Disease]
Record concept(s)
- nephrosis, congenital [MeSH concept]
- nephrotic syndrome, type 1 [MeSH concept]
- nephrotic syndrome, type 2 [MeSH concept]
- nephrotic syndrome, type 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Nephrotic Syndrome [NCIt concept]
- Congenital nephrotic syndrome [MedDRA Preferred Term]
- Congenital nephrotic syndrome [HPO term]
- Congenital nephrotic syndrome (disorder) [SNOMED CT concept]
- Familial nephrotic syndrome [MedDRA LLT]
- congenital nephrotic syndrome [Disease (Nov.)]
- familial nephrotic syndrome [DO Concept]
Validated automatic mappings to BTNT
- Congenital nephrotic syndrome, Finnish type [ORDO Disease]
- nephrotic syndrome type 1 [DO Concept]

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