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:
expandGenetic Diseases, X-Linked (D040181)
Parent Node:
expandHodgkin Disease (D006689)
..Starting node
..expandHodgkin disease, X-linked pseudoautosomal (C538326)

       Child Nodes:



 Sister Nodes: 
..expandHodgkin disease, X-linked pseudoautosomal (C538326)
..expandHodgkin Disease, Y-Linked Pseudoautosomal (C564034)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5234
Name:Hodgkin disease, X-linked pseudoautosomal
Definition:
Alternative IDs:OMIM:300221
ParentIDs:MESH:D006689|MESH:D040181
TreeNumbers:C04.557.386.355/C538326 |C15.604.515.569.355/C538326 |C16.320.322/C538326 |C20.683.515.761.355/C538326
Synonyms:HODGKIN DISEASE, X-LINKED PSEUDOAUTOSOMAL |LYMPHOMA, HODGKIN, X-LINKED PSEUDOAUTOSOMAL
Slim Mappings:Cancer|Genetic disease (inborn)|Immune system disease|Lymphatic disease
Reference: MedGen: C538326
MeSH: C538326
OMIM: 300221;

Genes:
Phenotypes
Disease Causing ClinVar Variants