Squamous cell carcinoma
Symptom Information:
Symptom ID: | HPO:0002860 | |||||
Synonyms: |
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Is a (Direct Parents): |
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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) Squamous cell carcinoma(HPO:0002860) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the skin(HPO:0008069) Squamous cell carcinoma(HPO:0002860) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Miscellaneous and site unspecified neoplasms malignant and unspecified(MedDRA:10027655) Neoplasms malignant site unspecified NEC(MedDRA:10029105) Squamous cell carcinoma(HPO:0002860) |
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Database Frequency: | 18 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Bloom syndrome | (Orphanet:125) |
Cheilitis glandularis | (Orphanet:1221) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3 | (OMIM:613988) |
Esophageal carcinoma | (Orphanet:70482) |
FANCONI ANEMIA, COMPLEMENTATION GROUP P | (OMIM:613951) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS | (OMIM:602540) |
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT | (OMIM:148210) |
KID syndrome | (Orphanet:477) |
LICHEN SCLEROSUS ET ATROPHICUS | (OMIM:151590) |
Melanoma-pancreatic cancer syndrome | (Orphanet:51013) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Squamous cell carcinoma of head and neck | (Orphanet:67037) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |
Xeroderma pigmentosum variant | (Orphanet:90342) |