Neoplasm of the skin
Symptom Information:
Symptom ID: | HPO:0008069 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Neoplasm of the skin(HPO:0008069) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the skin(HPO:0008069) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin and subcutaneous tissue disorders NEC(MedDRA:10040790) Skin and subcutaneous conditions NEC(MedDRA:10042356) Neoplasm of the skin(HPO:0008069) Skin neoplasms malignant and unspecified(MedDRA:10040900) Skin neoplasms malignant and unspecified (excl melanoma)(MedDRA:10040901) Neoplasm of the skin(HPO:0008069) |
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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) |