MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: disease of facial skeleton (MONDO:0023369)
Parent Node: mouth disease (MONDO:0006858)
Parent Node: sinusitis (MONDO:0005961)
..Starting node ..maxillary sinusitis ()
Child Nodes:
........acute maxillary sinusitis ()
........chronic maxillary sinusitis ()
Sister Nodes:
..chronic rhinosinusitis ()
..ethmoid sinusitis ()
..frontal sinusitis ()
..maxillary sinusitis ()
..sphenoid sinusitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5842
Name:	maxillary sinusitis
Definition:	An acute or chronic inflammatory process affecting the mucous membrane of the maxillary sinus.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal