FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 5
OrphanetNr:
OMIM Id: 616002
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0000089) Renal hypoplasia rare [HPO:skoehler] 78 / 7739
2
(HPO:0000097) Focal segmental glomerulosclerosis 37 / 7739
3
(HPO:0003774) Stage 5 chronic kidney disease rare [HPO:skoehler] 78 / 7739
4
(HPO:0000100) Nephrotic syndrome 83 / 7739
5
(HPO:0000093) Proteinuria 169 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: