Squamous cell carcinoma

Symptom Information:

Symptom ID: HPO:0002860
Synonyms:
Squamous cell carcinoma [OMIM:Squamous cell carcinoma]
Squamous cell carcinoma (1 patient) [OMIM:Squamous cell carcinoma (1 patient)]
Squamous cell carcinoma (skin and tongue) [OMIM:Squamous cell carcinoma (skin and tongue)]
Squamous cell carcinoma (skin or mucosa) [OMIM:Squamous cell carcinoma (skin or mucosa)]
Squamous cell carcinoma [MedDRA:10041823]
Quality:
Cross references:
OMIM: "Squamous cell carcinoma" [OMIM:Squamous cell carcinoma]
OMIM: "Squamous cell carcinoma (1 patient)" [OMIM:Squamous cell carcinoma (1 patient)]
OMIM: "Squamous cell carcinoma (skin and tongue)" [OMIM:Squamous cell carcinoma (skin and tongue)]
OMIM: "Squamous cell carcinoma (skin or mucosa)" [OMIM:Squamous cell carcinoma (skin or mucosa)]
Is a (Direct Parents):
HPO         Neoplasm of the skin
MedDRA Neoplasms malignant site unspecified NEC
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)
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)