Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expand
Neoplasms by Site (D009371)
Parent Node:
expand
Skin Diseases (D012871)
..Starting node
..expand
Skin Neoplasms (D012878)

       Child Nodes:
........expandAbdominal chemodectomas with cutaneous angiolipomas (C535552)
........expandAcanthoma (D049309)
........expandBazex-Dupre-Christol syndrome (C537663)
........expandBecker Nevus Syndrome (C565735)
........expandBlue rubber bleb nevus syndrome (C536240)
........expandCalcifying Epithelial Odontogenic Tumor (C537961)
........expandCardiomyopathy hypogonadism collagenoma syndrome (C535582)
........expandCollagenoma, Familial Cutaneous (C562925)
........expandDavenport Donlan syndrome (C535988)
........expandDermatopathia pigmentosa reticularis (C535374)
........expandFamilial cylindromatosis (C536611)
........expandFamilial multiple trichodiscomas (C536847)
........expandFanconi like syndrome (C536855)
........expandGiant pigmented hairy nevus (C536819)
........expandHamartoma, Precalcaneal Congenital Fibrolipomatous (C565226)
........expandHistiocytosis, Progressive Mucinous (C564186)
........expandMELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 (OMIM:155600)
........expandMELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 (OMIM:155601)
........expandMELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 (OMIM:609048)
........expandMELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 4 (OMIM:608035)
........expandMELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5 (OMIM:613099)
........expandMELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 7 (OMIM:612263)
........expandMELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8 (OMIM:614456)
........expandNevus, Epidermal (C562736)
........expandPALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL (OMIM:610644)
........expandPalmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal (C565693)
........expandPapillomatosis, Familial Cutaneous (C566832)
........expandPhacomatosis pigmentokeratotica (C537893)
........expandReactive angioendotheliomatosis (C535293)
........expandReed's syndrome (C535516)
........expandRombo syndrome (C535870)
........expandSchwannomatosis (C536641)
........expandSclerotylosis (C537526)
........expandSebaceous Gland Neoplasms (D012626) Child2
........expandSweat Gland Neoplasms (D013544)
........expandTrichoepithelioma, Multiple Familial, 2 (C567418)
........expandTrichoepitheliomas, Multiple Desmoplastic (C566034)
........expandTrichofolliculoma (C536553)
........expandTufted angioma (C536924)



 Sister Nodes: 
..expandAcneiform Eruptions (D017486) Child5
..expandAngiolymphoid Hyperplasia with Eosinophilia (D000796)
..expandBorrone Di Rocco Crovato syndrome (C536577)
..expandBoudhina Yedes Khiari syndrome (C537939)
..expandBreast Diseases (D001941) Child45
..expandC SYNDROME (OMIM:211750)
..expandCutaneous Fistula (D017577)
..expandDermatitis (D003872) Child57
..expandDermatoleukodystrophy (C538220)
..expandDermatomyositis (D003882) Child2
..expandEctodermal dysplasia/ skin fragility syndrome (C536183)
..expandElastosis perforans serpiginosa (C536202)
..expandElliott Ludman Teebi syndrome (C536204)
..expandErythema (D004890) Child19
..expandExanthema (D005076) Child1
..expandEyebrows duplication of, with stretchable skin and syndactyly (C536383)
..expandFACES syndrome (C536384)
..expandFacial Dermatoses (D005148) Child11
..expandFacial ectodermal dysplasia (C536385)
..expandFlynn Aird syndrome (C537066)
..expandFoot Diseases (D005534) Child13
..expandHair Diseases (D006201) Child174
..expandHand Dermatoses (D006229) Child1
..expandHernandez Fragoso syndrome (C536062)
..expandKeratoacanthoma (D007636) Child1
..expandKeratosis (D007642) Child149
..expandLeg Dermatoses (D007868)
..expandLipomatosis (D008068) Child11
..expandLupus Erythematosus, Cutaneous (D008178) Child3
..expandMacroepiphyseal dysplasia, McAlister Coe type (C537721)
..expandMASS syndrome (C536030)
..expandMastocytosis (D008415) Child9
..expandMedian cleft lip, corpus callosum, lipoma, and skin polyps (C536135)
..expandMental Retardation, Joint Hypermobility, And Skin Laxity, With Or Without Metabolic Abnormalities (C567209)
..expandMorgellons Disease (D055535)
..expandNail Diseases (D009260) Child42
..expandNecrobiotic Disorders (D017441) Child3
..expandNecrolytic Migratory Erythema (D058568)
..expandNephrogenic Fibrosing Dermopathy (D054989)
..expandOSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS (OMIM:612852)
..expandPanniculitis (D015434) Child6
..expandPhotosensitivity Disorders (D010787) Child31
..expandPigmentation Disorders (D010859) Child147
..expandPrurigo (D011536)
..expandPruritus (D011537) Child6
..expandPseudoatrophoderma Colli (C562909)
..expandPyoderma (D011711) Child3
..expandRosacea (D012393) Child1
..expandRoy Maroteaux Kremp syndrome (C535875)
..expandScalp Dermatoses (D012536) Child10
..expandScleredema Adultorum (D012592)
..expandScleroderma, Localized (D012594) Child5
..expandScleroderma, Systemic (D012595) Child7
..expandSebaceous Gland Diseases (D012625) Child12
..expandSkin Abnormalities (D012868) Child358
..expandSkin Diseases, Eczematous (D017443) Child35
..expandSkin Diseases, Genetic (D012873) Child462
..expandSkin Diseases, Infectious (D012874) Child103
..expandSkin Diseases, Metabolic (D012875) Child33
..expandSkin Diseases, Papulosquamous (D017444) Child26
..expandSkin Diseases, Vascular (D017445) Child33
..expandSkin Diseases, Vesiculobullous (D012872) Child54
..expandSkin Neoplasms (D012878) Child41
..expandSkin Ulcer (D012883) Child10
..expandSweat Gland Diseases (D013543) Child25
..expandUpton Young syndrome (C536473)
..expandXanthogranuloma, Juvenile (D014972)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10297
Name:Skin Neoplasms
Definition:Tumors or cancer of the SKIN.
Alternative IDs:
ParentIDs:MESH:D009371|MESH:D012871
TreeNumbers:C04.588.805 |C17.800.882
Synonyms:Cancer of Skin |Cancer of the Skin |Cancer, Skin |Cancers, Skin |Neoplasm, Skin |Neoplasms, Skin |Skin Cancer |Skin Cancers |Skin Neoplasm
Slim Mappings:Cancer|Skin disease
Reference: MedGen: D012878
MeSH: D012878
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants