Glomerulonephritis

Symptom Information:

Symptom ID: HPO:0000099
Synonyms:
Glomrulonephritis [HPO:0000099]
Glomerulonephritis [OMIM:Glomerulonephritis]
Glomrulonephritis [OMIM:Glomrulonephritis]
Glomerulonephritis [MedDRA:10018364]
Quality:
Cross references:
OMIM: "Glomerulonephritis" [OMIM:Glomerulonephritis]
OMIM: "Glomrulonephritis" [OMIM:Glomrulonephritis]
UMLS:C0017658 "Glomerulonephritis" [HPO:0000099]
Is a (Direct Parents):
MedDRA Immune and associated conditions NEC
HPO         Abnormality of the glomerulus
HPO         Nephritis
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 physiology(HPO:0012211)
                      Nephritis(HPO:0000123)
                         Glomerulonephritis(HPO:0000099)
                   Abnormal renal morphology(HPO:0012210)
                      Abnormality of the nephron(HPO:0012575)
                         Abnormality of the glomerulus(HPO:0000095)
                            Glomerulonephritis(HPO:0000099)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormal renal physiology(HPO:0012211)
                   Nephritis(HPO:0000123)
                      Glomerulonephritis(HPO:0000099)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Immune disorders NEC(MedDRA:10027665)
       Immune and associated conditions NEC(MedDRA:10027682)
          Glomerulonephritis(HPO:0000099)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY (OMIM:174770)
Alport syndrome (Orphanet:63)
Anti-glomerular basement membrane disease (Orphanet:375)
C3 glomerulonephritis (Orphanet:329931)
COMPLEMENT COMPONENT 4A DEFICIENCY (OMIM:614380)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Immunodeficiency with factor I anomaly (Orphanet:200418)
LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS (OMIM:247800)
Microcephaly - glomerulonephritis - marfanoid habitus (Orphanet:2172)
Nail-patella syndrome (Orphanet:2614)
Pediatric systemic lupus erythematosus (Orphanet:93552)
THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE (OMIM:314000)
Tubulointerstitial nephritis and uveitis syndrome (Orphanet:91500)