Thickening of the glomerular basement membrane

Symptom Information:

Symptom ID: HPO:0004722
Synonyms:
Thickening of the glomerular basement membrane [OMIM:Thickening of the glomerular basement membrane]
Thickening of the glomerular basement membrane (later in the disease) [OMIM:Thickening of the glomerular basement membrane (later in the disease)]
Quality:
Cross references:
OMIM: "Thickening of the glomerular basement membrane" [OMIM:Thickening of the glomerular basement membrane]
OMIM: "Thickening of the glomerular basement membrane (later in the disease)" [OMIM:Thickening of the glomerular basement membrane (later in the disease)]
Is a (Direct Parents):
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)
                            Thickening of the glomerular basement membrane(HPO:0004722)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Alport syndrome (Orphanet:63)
Atypical hemolytic uremic syndrome with DGKE deficiency (Orphanet:357008)
Autosomal dominant Alport syndrome (Orphanet:88918)
Autosomal recessive Alport syndrome (Orphanet:88919)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Immunodeficiency with factor H anomaly (Orphanet:200421)
Immunoglobulin-mediated membranoproliferative glomerulonephritis (Orphanet:329903)
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME (OMIM:308940)
Nephronophthisis 18 (OMIM:615862)
Nephronophthisis 3 (OMIM:604387)
Senior-Loken syndrome 9 (OMIM:616629)
X-linked Alport syndrome (Orphanet:88917)