Squamous cell carcinoma of the skin
Symptom Information:
Symptom ID: | HPO:0006739 | |||
Synonyms: |
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Cross references: |
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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) Squamous cell carcinoma of the skin(HPO:0006739) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the skin(HPO:0008069) Squamous cell carcinoma(HPO:0002860) Squamous cell carcinoma of the skin(HPO:0006739) MedDRA: |
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Database Frequency: | 6 / 7739 | |||
Resource: |
All diseases associated with this symptom:
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
Dyskeratosis congenita | (Orphanet:1775) |
EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED | (OMIM:305350) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |
Xeroderma pigmentosum complementation group C | (Orphanet:276255) |
Xeroderma pigmentosum complementation group E | (Orphanet:276261) |