Focal segmental glomerulosclerosis

Symptom Information:

Symptom ID: HPO:0000097
Synonyms:
Focal and segmental glomerular sclerosis [HPO:0000097]
Focal and segmental glomerulosclerosis [HPO:0000097]
focal glomerulosclerosis [HPO:0000097]
Focal and segmental glomerular sclerosis [OMIM:Focal and segmental glomerular sclerosis]
Focal and segmental glomerulosclerosis [OMIM:Focal and segmental glomerulosclerosis]
Focal glomerulosclerosis [OMIM:Focal glomerulosclerosis]
Focal segmental glomerulosclerosis [OMIM:Focal segmental glomerulosclerosis]
Focal glomerulosclerosis (in 33%) [OMIM:Focal glomerulosclerosis (in 33%)]
Focal segmental glomerulosclerosis (FSGS) [OMIM:Focal segmental glomerulosclerosis (FSGS)]
Focal segmental glomerulosclerosis (less common) [OMIM:Focal segmental glomerulosclerosis (less common)]
Focal segmental glomerulosclerosis [MedDRA:10067757]
Quality:
Cross references:
OMIM: "Focal and segmental glomerular sclerosis" [OMIM:Focal and segmental glomerular sclerosis]
OMIM: "Focal and segmental glomerulosclerosis" [OMIM:Focal and segmental glomerulosclerosis]
OMIM: "Focal glomerulosclerosis" [OMIM:Focal glomerulosclerosis]
OMIM: "Focal segmental glomerulosclerosis" [OMIM:Focal segmental glomerulosclerosis]
OMIM: "Focal glomerulosclerosis (in 33%)" [OMIM:Focal glomerulosclerosis (in 33%)]
OMIM: "Focal segmental glomerulosclerosis (FSGS)" [OMIM:Focal segmental glomerulosclerosis (FSGS)]
OMIM: "Focal segmental glomerulosclerosis (less common)" [OMIM:Focal segmental glomerulosclerosis (less common)]
Is a (Direct Parents):
HPO         Glomerulosclerosis
MedDRA Glomerulonephritis and nephrotic syndrome
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)
                               Focal segmental glomerulosclerosis(HPO:0000097)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Glomerulonephritis and nephrotic syndrome(MedDRA:10018365)
          Focal segmental glomerulosclerosis(HPO:0000097)
Database Frequency: 37 / 7739
Resource:

All diseases associated with this symptom:

Action myoclonus - renal failure syndrome (Orphanet:163696)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (Orphanet:93114)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Denys-Drash syndrome (Orphanet:220)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1 (OMIM:603278)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2 (OMIM:603965)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO (OMIM:607832)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO (OMIM:612551)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5 (OMIM:613237)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 (OMIM:614131)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7 (OMIM:616002)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8 (OMIM:616032)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9 (OMIM:616220)
Familial idiopathic steroid-resistant nephrotic syndrome (Orphanet:656)
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation (Orphanet:93214)
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes (Orphanet:93216)
Familial steroid-resistant nephrotic syndrome with sensorineural deafness (Orphanet:280406)
Frasier syndrome (Orphanet:347)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Galloway-Mowat syndrome (Orphanet:2065)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Hyperuricemia - anemia - renal failure (Orphanet:217330)
MELAS (Orphanet:550)
NEPHROTIC SYNDROME, TYPE 2 (OMIM:600995)
NEPHROTIC SYNDROME, TYPE 3 (OMIM:610725)
NEPHROTIC SYNDROME, TYPE 4 (OMIM:256370)
NEPHROTIC SYNDROME, TYPE 9 (OMIM:615573)
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS (OMIM:308990)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Proximal renal tubular acidosis (Orphanet:47159)
Renal cysts and diabetes syndrome (Orphanet:93111)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Spastic paraplegia - nephritis - deafness (Orphanet:2820)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)