MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandface disease (MONDO:0044987)
Parent Node:
expandsensory system disease (MONDO:0005128)
..Starting node
..expandnose disease ()

       Child Nodes:
........expandepistaxis ()
........expandnasal cavity and paranasal sinus lethal midline granuloma ()
........expandnasal cavity disease ()
........expandnasal dermoid cyst ()
........expandparanasal sinus disease ()



 Sister Nodes: 
..expandauditory system disease ()
..expanddisease of ear ()
..expanddisease of visual system ()
..expandHolmes-Adie syndrome ()
..expandnose disease ()
..expandprogressive external ophthalmoplegia ()
..expandsensory organ benign neoplasm ()
..expandsensory system cancer ()
..expandtongue disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:2436
Name:nose disease
Definition:A disease involving the nose.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:disease of nose; disease or disorder of nose; disorder of nose; disorder of nose; disorder of the nose; nasal disorder; nose disease; nose disease or disorder
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal