MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandskin disease (MONDO:0005093)
..Starting node
..expandother acquired skin disease ()

       Child Nodes:
........expandacquired kinky hair syndrome ()
........expandBazex syndrome ()
........expandbullous impetigo ()
........expandcheilitis glandularis ()
........expandcorticosteroid-sensitive aseptic abscess syndrome ()
........expandcutaneous pseudolymphoma ()
........expanderosive pustular dermatosis of the scalp ()
........expandinfective dermatitis associated with HTLV-1 ()
........expandinterstitial granulomatous dermatitis with arthritis ()
........expandJessner lymphocytic infiltration of the skin ()
........expandKerion celsi ()
........expandnephrogenic systemic fibrosis ()
........expandoral erosive lichen ()
........expandpellagra ()
........expandprimary cutaneous plasmacytosis ()
........expandscleredema ()
........expandSneddon syndrome ()
........expandsubcorneal pustular dermatosis ()
........expandsweet syndrome ()
........expandvirus-associated trichodysplasia spinulosa ()
........expandWells syndrome ()



 Sister Nodes: 
..expandAchenbach syndrome ()
..expandaquagenic pruritus ()
..expandautoimmune disease with skin involvement ()
..expandBorrone di Rocco Crovato syndrome ()
..expandchronic ulcer of skin ()
..expandcutaneous mucinosis ()
..expandcutaneous sclerosis ()
..expanddermatitis ()
..expandepidermal appendage anomaly ()
..expanderythema multiforme ()
..expanderythematosquamous dermatosis ()
..expandexanthem (disease) ()
..expandfacial dermatosis ()
..expandgenetic photodermatosis ()
..expandgenetic skin disease ()
..expandhand dermatosis ()
..expandhematohidrosis ()
..expandhordeolum ()
..expandhyperglobulinemic purpura ()
..expandimmune deficiency with skin involvement ()
..expandinflammatory skin disease ()
..expandkeratosis ()
..expandkeratosis pilaris ()
..expandKimura disease ()
..expandleg dermatosis ()
..expandlichen disease ()
..expandlipodystrophy (disease) ()
..expandlivedoid vasculopathy ()
..expandmetabolic disease with skin involvement ()
..expandmongolian spot ()
..expandnecrobiosis lipoidica ()
..expandnon-neoplastic nevus ()
..expandother acquired skin disease ()
..expandother genetic dermis disorder ()
..expandother genetic epidermal disease ()
..expandparonychia (disease) ()
..expandpityriasis rotunda ()
..expandpremature aging ()
..expandprurigo nodularis ()
..expandpyoderma ()
..expandrare epidermal disease ()
..expandrare photodermatosis ()
..expandreactive cutaneous fibrous lesion ()
..expandrosacea ()
..expandscalp dermatosis ()
..expandsclerema neonatorum ()
..expandsebaceous gland disease ()
..expandsevere cutaneous adverse reaction ()
..expandskin atrophy ()
..expandskin disease caused by infection ()
..expandskin neoplasm ()
..expandskin pigmentation disease ()
..expandskin sarcoidosis ()
..expandskin vascular disease ()
..expandsunburn ()
..expandsweat gland disease ()
..expandtoxic dermatosis ()
..expandunclassified genetic skin disorder ()
..expandvesiculobullous skin disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19546
Name:other acquired skin disease
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal