Diffuse mesangial sclerosis

Symptom Information:

Symptom ID: HPO:0001967
Synonyms:
Diffuse mesangial sclerosis glomerulopathy [HPO:0001967]
Mesangial sclerosis [HPO:0001967]
Diffuse mesangial sclerosis [OMIM:Diffuse mesangial sclerosis]
Diffuse mesangial sclerosis glomerulopathy [OMIM:Diffuse mesangial sclerosis glomerulopathy]
Mesangial sclerosis [OMIM:Mesangial sclerosis]
Diffuse mesangial sclerosis (less common) [OMIM:Diffuse mesangial sclerosis (less common)]
Diffuse mesangial sclerosis [MedDRA:10054832]
Quality:
Cross references:
OMIM: "Diffuse mesangial sclerosis" [OMIM:Diffuse mesangial sclerosis]
OMIM: "Diffuse mesangial sclerosis glomerulopathy" [OMIM:Diffuse mesangial sclerosis glomerulopathy]
OMIM: "Mesangial sclerosis" [OMIM:Mesangial sclerosis]
OMIM: "Diffuse mesangial sclerosis (less common)" [OMIM:Diffuse mesangial sclerosis (less common)]
Is a (Direct Parents):
MedDRA Nephropathies and tubular disorders NEC
HPO         Mesangial abnormality
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)
                            Mesangial abnormality(HPO:0001966)
                               Diffuse mesangial sclerosis(HPO:0001967)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Nephropathies and tubular disorders NEC(MedDRA:10029150)
          Diffuse mesangial sclerosis(HPO:0001967)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Denys-Drash syndrome (Orphanet:220)
Familial idiopathic steroid-resistant nephrotic syndrome (Orphanet:656)
Familial steroid-resistant nephrotic syndrome with sensorineural deafness (Orphanet:280406)
Galloway-Mowat syndrome (Orphanet:2065)
MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES (OMIM:249660)
NEPHROTIC SYNDROME, TYPE 3 (OMIM:610725)
NEPHROTIC SYNDROME, TYPE 4 (OMIM:256370)
NEPHROTIC SYNDROME, TYPE 8 (OMIM:615244)
Pierson syndrome (Orphanet:2670)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)