MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: other acquired skin disease (MONDO:0019546)
Parent Node: rheumatologic disorder (MONDO:0005554)
..Starting node ..interstitial granulomatous dermatitis with arthritis ()
Child Nodes:
Sister Nodes:
..acroosteolysis dominant type ()
..arthritis ()
..autoinflammatory syndrome ()
..camptodactyly-arthropathy-coxa vara-pericarditis syndrome ()
..fibroblastic rheumatism ()
..Gorham-Stout disease ()
..idiopathic juvenile osteoporosis ()
..immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome ()
..intermittent hydrarthrosis ()
..interstitial granulomatous dermatitis with arthritis ()
..isolated sternocostoclavicular hyperostosis ()
..lupus erythematosus ()
..mixed connective tissue disease ()
..palindromic rheumatism ()
..polymyalgia rheumatica ()
..progeria-associated arthropathy ()
..rheumatic disease of mitral valve ()
..rheumatic pulmonary valve disease ()
..scleroderma (disease) ()
..sweet syndrome ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	19199
Name:	interstitial granulomatous dermatitis with arthritis
Definition:	Interstitial granulomatous dermatitis with arthritis is a rare rheumatologic disease characterized by the occurrence of inflammatory arthritis in association with large, erythematous, symmetrical cutaneous lesions (ranging from typical, but infrequent, cord-like lesions on the flanks to more common violaceous plaques on the trunk and limbs) featuring a typical histologic infiltrate mainly constituted of histiocytes.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Ackerman dermatitis syndrome; IGDA
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal