MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: chronic rhinosinusitis (MONDO:0006031)
Parent Node: sphenoid sinusitis (MONDO:0005964)
..Starting node ..chronic sphenoidal sinusitis ()
Child Nodes:
Sister Nodes:
..acute sphenoidal sinusitis ()
..chronic sphenoidal sinusitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1123
Name:	chronic sphenoidal sinusitis
Definition:	Inflammation of the sphenoid sinus that typically lasts beyond eight weeks. It is caused by infections, allergies, and the presence of sinus polyps or a deviated septum. Signs and symptoms include headache, nasal discharge, swelling in the face, dizziness, and breathing difficulties.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	chronic sphenoid sinusitis; sphenoid sinusitis, chronic; sphenoidal sinus-chr.
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal