Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandPolycystic Kidney, Autosomal Recessive (D017044)
..Starting node
..expandRenal dysplasia diffuse cystic (C537755)

       Child Nodes:



 Sister Nodes: 
..expandPolycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia (C564881)
..expandPolycystic kidneys, severe infantile with tuberous sclerosis (C536328)
..expandRenal dysplasia diffuse cystic (C537755)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9650
Name:Renal dysplasia diffuse cystic
Definition:
Alternative IDs:
ParentIDs:MESH:D017044
TreeNumbers:C12.777.419.403.875.510/C537755 |C13.351.968.419.403.875.510/C537755 |C16.320.793/C537755
Synonyms:Diffuse cystic renal dysplasia |Renal Dysplasia, Diffuse Cystic
Slim Mappings:Genetic disease (inborn)|Urogenital disease (female)|Urogenital disease (male)
Reference: MedGen: C537755
MeSH: C537755
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants