Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandRenal Insufficiency, Chronic (D051436)
..Starting node
..expandKidney Failure, Chronic (D007676)

       Child Nodes:
........expandFrasier Syndrome (D052159)
........expandNephropathy deafness hyperparathyroidism (C536401)
........expandNephropathy, Progressive, with Deafness (C563713)



 Sister Nodes: 
..expandKidney Failure, Chronic (D007676) Child3
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6097
Name:Kidney Failure, Chronic
Definition:The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION.
Alternative IDs:
ParentIDs:MESH:D051436
TreeNumbers:C12.777.419.780.750.500 |C13.351.968.419.780.750.500
Synonyms:Chronic Kidney Failure |Chronic Renal Failure |Disease, End-Stage Kidney |Disease, End-Stage Renal |End Stage Kidney Disease |End-Stage Kidney Disease |End Stage Renal Disease |End-Stage Renal Disease |End-Stage Renal Failure |ESRD |Kidney Disease, End-Stage |Renal
Slim Mappings:Urogenital disease (female)|Urogenital disease (male)
Reference: MedGen: D007676
MeSH: D007676
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants