Focal segmental glomerulosclerosis 10

Preferred Label : Focal segmental glomerulosclerosis 10;

Symbol : FSGS10;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Glomerular basement membrane disease, nail-patella syndrome type; Glomerulosclerosis, focal segmental, 10; Nail-patella-like renal disease; NPLRD;

Inheritance : Autosomal recessive;

Prefixed ID : #256020;

Details

Origin ID

256020;

UMLS CUI

C0403548;

Currated CISMeF NLP mapping
- Nail patella-like renal disease (disorder) [SNOMED CT concept]
- Nail-patella-like renal disease [ORDO Disease]
- Salcedo syndrome [MeSH concept]
- salcedo syndrome [MeSH Supplementary Concept]
Genes related to phenotype
- Lim homeobox transcription factor 1, beta [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Focal segmental glomerulosclerosis [HPO term]
- Juvenile onset [HPO term]
- Late onset [HPO term]
- Middle age onset [HPO term]
- Minimal change glomerulonephritis [HPO term]
- Proteinuria [HPO term]
- Renal insufficiency [HPO term]
- Stage 5 chronic kidney disease [HPO term]
- Young adult onset [HPO term]
ORDO concept(s)
- Nail-patella-like renal disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Nail patella-like renal disease (disorder) [SNOMED CT concept]
- Nail-patella-like renal disease [ORDO Disease]
- Salcedo syndrome [MeSH concept]
- salcedo syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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