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: sinusitis (MONDO:0005961)
..Starting node ..chronic rhinosinusitis ()
Child Nodes:
........chronic ethmoidal sinusitis ()
........chronic frontal sinusitis ()
........chronic maxillary sinusitis ()
........chronic sphenoidal 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:	6031
Name:	chronic rhinosinusitis
Definition:	Chronic form of sinusitis.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	chronic sinusitis; sinusitis, chronic
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal