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: nasopharyngitis (MONDO:0001040)
..Starting node ..common cold ()
Child Nodes:
Sister Nodes:
..adenoiditis ()
..common cold ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5709
Name:	common cold
Definition:	An inflammatory process affecting the nasal mucosa, usually caused by viruses (e.g., rhinovirus, adenovirus, parainfluenza virus, and coronavirus). It is characterized by chills, headaches, mucopurulent nasal discharge, coughing, and facial pain.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	acute coryza; acute nasopharyngitis; acute nasopharyngitis [common cold]; acute rhinitis; acute viral rhinopharyngitis; nasopharyngitis - acute; nasopharyngitis, acute; rhino-sinusitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: HAVCR1; IL21R; IL4R; MS4A2; PHF11; PLA2G7; SELP; SPINK5;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal