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:
expandObesity (D009765)
Parent Node:
expandWAGR Syndrome (D017624)
..Starting node
..expandWilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome (C567292)

       Child Nodes:



 Sister Nodes: 
..expandChromosome 11p Deletion Syndrome (C541598)
..expandWilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome (C567292)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:11761
Name:Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome
Definition:
Alternative IDs:OMIM:612469
ParentIDs:MESH:D009765|MESH:D017624
TreeNumbers:C04.557.435.595.950/C567292 |C04.588.945.947.535.585.950/C567292 |C04.700.635.950/C567292 |C10.597.606.643.969/C567292 |C11.250.060.950/C567292 |C11.270.060.950/C567292 |C11.941.375.060.950/C567292 |C12.706.316.096.875/C567292 |C12.758.820.750.585.950/C567292 |C1
Synonyms:Chromosome 11p13-P12 Deletion Syndrome |WAGRO |WAGRO Syndrome |WAGR Syndrome With Obesity
Slim Mappings:Cancer|Congenital abnormality|Endocrine system disease|Eye disease|Genetic disease (inborn)|Nervous system disease|Nutrition disorder|Signs and symptoms|Urogenital disease (female)|Urogenital disease (male)
Reference: MedGen: C567292
MeSH: C567292
OMIM: 612469;

Genes: AF8T;
Phenotypes
Disease Causing ClinVar Variants