Basal cell carcinoma
Symptom Information:
Symptom ID: | HPO:0002671 | ||||||||
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) Basal cell carcinoma(HPO:0002671) Neoplasm(HPO:0002664) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the skin(HPO:0008069) Basal cell carcinoma(HPO:0002671) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin neoplasms malignant and unspecified(MedDRA:10040900) Skin neoplasms malignant and unspecified (excl melanoma)(MedDRA:10040901) Basal cell carcinoma(HPO:0002671) |
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Database Frequency: | 18 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1 | (OMIM:605462) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
Constitutional mismatch repair deficiency syndrome | (Orphanet:252202) |
EPIDERMODYSPLASIA VERRUCIFORMIS | (OMIM:226400) |
Epidermodysplasia verruciformis | (Orphanet:302) |
Familial multiple trichoepithelioma | (Orphanet:867) |
Gorlin syndrome | (Orphanet:377) |
LMNA-related cardiocutaneous progeria syndrome | (Orphanet:363618) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Muir-Torre syndrome | (Orphanet:587) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Rombo syndrome | (Orphanet:3110) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |
Xeroderma pigmentosum complementation group C | (Orphanet:276255) |
Xeroderma pigmentosum complementation group E | (Orphanet:276261) |
Xeroderma pigmentosum variant | (Orphanet:90342) |