Basal cell carcinoma

Symptom Information:

Symptom ID: HPO:0002671
Synonyms:
Basal cell carcinomas [HPO:0002671]
Basal cell epithelioma [HPO:0002671]
Basal cell nevus [HPO:0002671]
Basalioma [HPO:0002671]
Basal cell carcinoma [OMIM:Basal cell carcinoma]
Basal cell carcinomas [OMIM:Basal cell carcinomas]
Basal cell nevi [OMIM:Basal cell nevi]
Basal cell carcinoma [MedDRA:10004146]
Quality:
Cross references:
OMIM: "Basal cell carcinoma" [OMIM:Basal cell carcinoma]
OMIM: "Basal cell carcinomas" [OMIM:Basal cell carcinomas]
OMIM: "Basal cell nevi" [OMIM:Basal cell nevi]
Is a (Direct Parents):
HPO         Basalioma of the outer ear
MedDRA Skin neoplasms malignant and unspecified (excl melanoma)
HPO         Neoplasm of the skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Neoplasm of the skin(HPO:0008069)
                Basal cell carcinoma(HPO:0002671)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             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)
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)