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: lymph node disease (MONDO:0004928)
..Starting node ..lymphadenitis (disease) ()
Child Nodes:
........axillary lymphadenitis ()
........cat-scratch disease ()
........cervical lymphadenitis ()
........Kikuchi-Fujimoto disease ()
........mesenteric lymphadenitis ()
........mucocutaneous lymph node syndrome ()
........postauricular lymphadenitis ()
........sialadenitis ()
........suppurative lymphadenitis ()
Sister Nodes:
..glandular tularemia ()
..lymph node neoplasm ()
..lymph node tuberculosis ()
..lymphadenitis (disease) ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2052
Name:	lymphadenitis (disease)
Definition:	Acute or chronic inflammation of one or more lymph nodes. It is usually caused by an infectious process.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	acute adenitis; acute lymphadenitis; adenitis; chronic adenitis; chronic lymphadenitis; Inflammation of lymph node; inflammation of lymph node; lymph gland infection; lymph node inflammation; lymph nodeitis; lymphadenitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal