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: head disease (MONDO:0005042)
Parent Node: lymphadenitis (disease) (MONDO:0002052)
..Starting node ..postauricular lymphadenitis ()
Child Nodes:
Sister Nodes:
..axillary lymphadenitis ()
..cat-scratch disease ()
..cervical lymphadenitis ()
..Kikuchi-Fujimoto disease ()
..mesenteric lymphadenitis ()
..mucocutaneous lymph node syndrome ()
..postauricular lymphadenitis ()
..sialadenitis ()
..suppurative lymphadenitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3068
Name:	postauricular lymphadenitis
Definition:	Inflammation of the postauricular lymph nodes.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	lymphadenitis (disease) of mastoid lymph node; mastoid lymph node lymphadenitis (disease)
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal