Glomerulosclerosis

Symptom Information:

Symptom ID: HPO:0000096
Synonyms:
Glomerulosclerosis [OMIM:Glomerulosclerosis]
Glomerulosclerosis [MedDRA:10061989]
Quality:
Cross references:
OMIM: "Glomerulosclerosis" [OMIM:Glomerulosclerosis]
Is a (Direct Parents):
MedDRA Nephropathies and tubular disorders NEC
HPO         Abnormality of the glomerulus
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal morphology(HPO:0012210)
                      Abnormality of the nephron(HPO:0012575)
                         Abnormality of the glomerulus(HPO:0000095)
                            Glomerulosclerosis(HPO:0000096)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Nephropathies and tubular disorders NEC(MedDRA:10029150)
          Glomerulosclerosis(HPO:0000096)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (Orphanet:34149)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
COENZYME Q10 DEFICIENCY, PRIMARY, 1 (OMIM:607426)
Dent disease type 1 (Orphanet:93622)
Fabry disease (Orphanet:324)
Familial dysautonomia (Orphanet:1764)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE (OMIM:310468)
OCULORENOCEREBELLAR SYNDROME (OMIM:257970)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Tyrosinemia type 1 (Orphanet:882)