Neoplasm of the skin

Symptom Information:

Symptom ID: HPO:0008069
Synonyms:
Dermatological tumors [HPO:0008069]
Neoplasia of the skin [HPO:0008069]
Skin tumors [HPO:0008069]
Skin tumor [Orphanet:23680]
Neoplasm of skin [HPO:0008069]
Neoplasm of skin (disorder) [Orphanet:23680]
Mass of skin (finding) [Orphanet:23680]
Skin Neoplasms [Orphanet:23680]
Mass of skin [Orphanet:23680]
Skin tumors [OMIM:Skin tumors]
Skin tumors/lumps/epidermal cysts [Orphanet:23680]
Neoplasm skin [Orphanet:23680]
Skin mass [Orphanet:23680]
Neoplasm skin [MedDRA:10029098]
Neoplasm of uncertain behavior of skin [MedDRA:10029098]
Neoplasm of uncertain behaviour of skin [MedDRA:10029098]
Skin growth NOS [MedDRA:10029098]
Skin neoplasm NOS [MedDRA:10029098]
Skin tumor [MedDRA:10029098]
Skin tumor NOS [MedDRA:10029098]
Skin tumor-like condition NOS [MedDRA:10029098]
Tumor of epidermal appendage NOS [MedDRA:10029098]
Tumor of the dermis NOS [MedDRA:10029098]
Tumor of the epidermis NOS [MedDRA:10029098]
Tumor-like skin condition (NOS) [MedDRA:10029098]
Tumor-like skin condition NOS [MedDRA:10029098]
Tumour-like skin condition NOS [MedDRA:10029098]
Skin tumor-like condition (NOS) [MedDRA:10029098]
Skin tumour [MedDRA:10029098]
Skin mass [MedDRA:10067868]
Fibrous nodule [MedDRA:10067868]
Nodule skin [MedDRA:10067868]
Nodule subcutaneous [MedDRA:10067868]
Phyma [MedDRA:10067868]
Skin nodule [MedDRA:10067868]
Subcutaneous nodule [MedDRA:10067868]
Fibrous nodules [OMIM:Fibrous nodules]
Subcutaneous nodules (fingers) [OMIM:Subcutaneous nodules (fingers)]
Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial) [OMIM:Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial)]
Epidermal cyst [MedDRA:10014983]
Epidermoid cyst [Orphanet:23680]
Epidermoid cyst (morphologic abnormality) [Orphanet:23680]
Sebaceous cyst (morphologic abnormality) [Orphanet:23680]
Keratinizing cyst (disorder) [Orphanet:23680]
Epidermoid cyst (disorder) [Orphanet:23680]
Epidermal inclusion cyst (morphologic abnormality) [Orphanet:23680]
Epidermoid cyst of skin (disorder) [Orphanet:23680]
Keratinizing cyst (morphologic abnormality) [Orphanet:23680]
Epithelial inclusion cyst (morphologic abnormality) [Orphanet:23680]
Epithelial inclusion cyst [Orphanet:23680]
Epithelial cyst [Orphanet:23680]
Sebaceous cysts (buttocks and perineum) [OMIM:Sebaceous cysts (buttocks and perineum)]
Quality:
Cross references:
Orphanet:23680 "Skin tumors/lumps/epidermal cysts" [Orphanet:23680]
OMIM: "Skin tumors" [OMIM:Skin tumors]
OMIM: "Fibrous nodules" [OMIM:Fibrous nodules]
OMIM: "Subcutaneous nodules (fingers)" [OMIM:Subcutaneous nodules (fingers)]
OMIM: "Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial)" [OMIM:Subcutaneous nodules (interphalangeal joints, knees, feet, elbows, pretibial)]
OMIM: "Sebaceous cysts (buttocks and perineum)" [OMIM:Sebaceous cysts (buttocks and perineum)]
UMLS:C0037286 "Skin Neoplasms" [Orphanet:23680]
UMLS:C0281981 "Mass of skin" [Orphanet:23680]
UMLS:C0259770 "Epithelial inclusion cyst" [Orphanet:23680]
UMLS:C0014511 "Epithelial cyst" [Orphanet:23680]
Is a (Direct Parents):
HPO         Merkel cell skin cancer
HPO         Fibrofolliculoma
HPO         Neoplasm by anatomical site
HPO         Cutaneous myxoma
Orphanet Abnormality of the skin
HPO         Abnormality of the skin
MedDRA Skin neoplasms malignant and unspecified (excl melanoma)
MedDRA Skin and subcutaneous conditions NEC
HPO         Papilloma
HPO         Skin adnexal neoplasm
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skin(HPO:0008069)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Neoplasm of the skin(HPO:0008069)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin neoplasms malignant and unspecified(MedDRA:10040900)
       Skin neoplasms malignant and unspecified (excl melanoma)(MedDRA:10040901)
          Neoplasm of the skin(HPO:0008069)
    Skin and subcutaneous tissue disorders NEC(MedDRA:10040790)
       Skin and subcutaneous conditions NEC(MedDRA:10042356)
          Neoplasm of the skin(HPO:0008069)
Database Frequency: 84 / 7739
Resource:

All diseases associated with this symptom:

Bazex-Dupré-Christol syndrome (Orphanet:113)
Bloom syndrome (Orphanet:125)
Carney complex (Orphanet:1359)
Cartilage-hair hypoplasia (Orphanet:175)
Cheilitis glandularis (Orphanet:1221)
Classical mycosis fungoides (Orphanet:2584)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Cowden syndrome (Orphanet:201)
Dermatofibrosarcoma protuberans (Orphanet:31112)
Desmoid tumor (Orphanet:873)
Disseminated superficial actinic porokeratosis (Orphanet:79152)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Embryonary disorganization syndrome (Orphanet:1664)
Epidermodysplasia verruciformis (Orphanet:302)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Erosive pustular dermatosis of the scalp (Orphanet:222)
Erythrokeratodermia variabilis (Orphanet:317)
FLOTCH syndrome (Orphanet:2045)
Familial cylindromatosis (Orphanet:211)
Familial keratoacanthoma (Orphanet:493)
Familial leiomyomatosis (Orphanet:523)
Familial multiple fibrofolliculoma (Orphanet:338)
Familial multiple trichoepithelioma (Orphanet:867)
Focal dermal hypoplasia (Orphanet:2092)
Gorlin syndrome (Orphanet:377)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary progressive mucinous histiocytosis (Orphanet:158025)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hyperkeratosis lenticularis perstans (Orphanet:409)
KID syndrome (Orphanet:477)
Kindler syndrome (Orphanet:2908)
Large congenital melanocytic nevus (Orphanet:626)
Li-Fraumeni syndrome (Orphanet:524)
Linear verrucous nevus syndrome (Orphanet:2611)
MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY (OMIM:259600)
Muir-Torre syndrome (Orphanet:587)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Neurofibromatosis type 1 (Orphanet:636)
Neurofibromatosis type 2 (Orphanet:637)
Nevus comedonicus syndrome (Orphanet:64754)
Non-polyposis Turcot syndrome (Orphanet:99817)
Oculocerebrorenal syndrome (Orphanet:534)
Oculocutaneous albinism (Orphanet:55)
Oculocutaneous albinism type 1A (Orphanet:79431)
Oculocutaneous albinism type 1B (Orphanet:79434)
Oculocutaneous albinism type 2 (Orphanet:79432)
Oculocutaneous albinism type 4 (Orphanet:79435)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Oral erosive lichen (Orphanet:31142)
Pachydermoperiostosis (Orphanet:2796)
Pachyonychia congenita (Orphanet:2309)
Palmoplantar keratoderma-sclerodactyly syndrome (Orphanet:384)
Papillon-Lefèvre syndrome (Orphanet:678)
Piebald trait - neurologic defects (Orphanet:2885)
Piebaldism (Orphanet:2884)
Porokeratosis (Orphanet:79358)
Porokeratosis of Mibelli (Orphanet:735)
Porokeratosis plantaris palmaris et disseminata (Orphanet:737)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Proliferating trichilemmal cyst (Orphanet:492)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Rombo syndrome (Orphanet:3110)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Sebocystomatosis (Orphanet:841)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Steatocystoma multiplex - natal teeth (Orphanet:3184)
Syringocystadenoma papilliferum (Orphanet:840)
Sézary syndrome (Orphanet:3162)
TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC (OMIM:190345)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Tumoral calcinosis (Orphanet:53715)
Werner syndrome (Orphanet:902)
X-linked recessive ocular albinism (Orphanet:54)
Xeroderma pigmentosum (Orphanet:910)
Xeroderma pigmentosum complementation group F (Orphanet:276264)
Xeroderma pigmentosum variant (Orphanet:90342)
Xeroderma pigmentosum/Cockayne syndrome complex (Orphanet:220295)