Nphs2 stomatin family member, podocin

Preferred Label : Nphs2 stomatin family member, podocin;

Symbol : NPHS2;

CISMeF acronym : NPHS2;

Type : Gene;

Alternative titles and symbols : PDCN; Podocin;

Ensembl ID : ENSG00000116218;

Prefixed ID : *604766;

Details

Origin ID

604766;

UMLS CUI

C1421972;

Automatic exact mappings (from CISMeF team)
- NPHS2 protein [MeSH Supplementary Concept]
- NPHS2 stomatin family member, podocin [ORDO Gene]
- Podocin [NCIt concept]
Currated CISMeF NLP mapping
- NPHS2 Gene [NCIt concept]
- NPHS2 gene [LOINC component]
- NPHS2 stomatin family member, podocin [HGNC gene]
HGNC gene
- NPHS2 stomatin family member, podocin [HGNC gene]
NCIt concept(s)
- NPHS2 Gene [NCIt concept]
- NPHS2 wt Allele [NCIt concept]
- Podocin [NCIt concept]
ORDO concept(s)
- NPHS2 stomatin family member, podocin [ORDO Gene]
Phenotypes related
- Nephrotic syndrome, type 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NPHS2 Gene [NCIt concept]
- NPHS2 gene [LOINC component]
- NPHS2 stomatin family member, podocin [HGNC gene]
Validated automatic mappings to BTNT
- NPHS2 wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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