MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Disease Browser
Parent Node:
expandneoplasm (disease) (MONDO:0005070)
Parent Node:
expandskin disease (MONDO:0005093)
..Starting node
..expandskin neoplasm ()

       Child Nodes:
........expandactinic keratosis (disease) ()
........expandbenign dermal neurilemmoma ()
........expandbenign neoplasm of skin ()
........expandcalcifying epithelial odontogenic tumor ()
........expandcutaneous ganglioneuroma ()
........expanddermis tumor ()
........expanddermoid cyst of skin ()
........expandepidermal appendage tumor ()
........expandepithelial skin neoplasm ()
........expandeyelid neoplasm ()
........expandfamilial Dupuytren contracture ()
........expandhemangiopericytoma of skin ()
........expandinherited skin tumor ()
........expandmelanocytic skin neoplasm ()
........expandskin cancer ()
........expandskin tag ()



 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:2531
Name:skin neoplasm
Definition:A benign or malignant tumor involving the skin. Representative examples of benign skin neoplasms include the benign melanocytic skin nevus, acanthoma, sebaceous adenoma, sweat gland adenoma, lipoma, hemangioma, fibroma, and benign fibrous histiocytoma. Representative examples of malignant skin neoplasms include basal cell carcinoma, squamous cell carcinoma, melanoma, and Kaposi sarcoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:neoplasm of skin; neoplasm of skin by site; neoplasm of the skin; neoplasm of zone of skin; skin; skin benign neoplasm; skin neoplasm; skin neoplasms; skin tumor; tumor of skin; tumor of the skin; tumor of zone of skin; zone of skin neoplasm; zone of skin neoplasm (disease); zone of skin tumor
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: MRPS22;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal