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:
expandintegumentary system disease (MONDO:0002051)
..Starting node
..expandskin disease ()

       Child 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 ()



 Sister Nodes: 
..expandBartholin duct cyst ()
..expandBartholin gland neoplasm ()
..expandbenign mammary dysplasia ()
..expandbreast fibrocystic disease ()
..expandcervical aortic arch ()
..expandcorneal disease ()
..expandcutaneous mycosis ()
..expanddemodicidosis ()
..expanddermis disease ()
..expanddisease of pilosebaceous unit ()
..expandintegumentary system benign neoplasm ()
..expandintegumentary system cancer ()
..expandkeratinization disease ()
..expandlip disease ()
..expandnail disease ()
..expandneoplasm of aortic body ()
..expandpanniculitis ()
..expandpseudoxanthoma elasticum (inherited or acquired) ()
..expandskin appendage disease ()
..expandskin disease ()
..expandsubcutaneous tissue disease ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:5093
Name:skin disease
Definition:Any deviation from the normal structure or function of the skin or subcutaneous tissue that is manifested by a characteristic set of symptoms and signs.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:cutaneous disorder; dermatosis; disease of zone of skin; disease or disorder of zone of skin; disorder of skin; disorder of zone of skin; disorder of zone of skin; genodermatosis; skin and subcutaneous tissue disease; skin diseases and manifestations; skin disorder; zone of skin disease; zone of ski
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal