NPHS2 stomatin family member, podocin

Preferred Label : NPHS2 stomatin family member, podocin;

Approved symbol HGNC : NPHS2;

Alias symbols HGNC : SRN1; PDCN;

Chromosome HGNC : 1q25.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000116218;

Details

Origin ID

HGNC:13394;

UMLS CUI

C1421972;

Automatic exact mappings (from CISMeF team)
- NPHS2 stomatin family member, podocin [ORDO Gene]
- Nephrotic syndrome, type 2 [OMIM Phenotype]
Currated CISMeF NLP mapping
- NPHS2 Gene [NCIt concept]
- NPHS2 gene [LOINC component]
- Nphs2 stomatin family member, podocin [OMIM gene]
NCIt concept
- NPHS2 Gene [NCIt concept]
OMIM gene
- Nphs2 stomatin family member, podocin [OMIM gene]
Orphanet gene
- NPHS2 stomatin family member, podocin [ORDO Gene]
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 [OMIM gene]

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