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: inflammatory disease (MONDO:0021166)
Parent Node: paranasal sinus disease (MONDO:0001735)
..Starting node ..sinusitis ()
Child Nodes:
........chronic rhinosinusitis ()
........ethmoid sinusitis ()
........frontal sinusitis ()
........maxillary sinusitis ()
........sphenoid sinusitis ()
Sister Nodes:
..maxillary sinus cholesteatoma ()
..paranasal sinus neoplasm (disease) ()
..sinusitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5961
Name:	sinusitis
Definition:	An acute or chronic inflammatory process affecting the mucous membranes of any sinus cavity.
Alternative IDs:
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Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal