Cutaneous melanoma
Symptom Information:
Symptom ID: | HPO:0012056 | ||||
Synonyms: |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Neoplasm(HPO:0002664) Neoplasm by histology(HPO:0011792) Melanoma(HPO:0002861) Cutaneous melanoma(HPO:0012056) Neoplasm by anatomical site(HPO:0011793) Neoplasm of the skin(HPO:0008069) Cutaneous melanoma(HPO:0012056) Abnormality of the integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Neoplasm of the skin(HPO:0008069) Cutaneous melanoma(HPO:0012056) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
BAP1-related tumor predisposition syndrome | (Orphanet:289539) |
Familial melanoma | (Orphanet:618) |
Large congenital melanocytic nevus | (Orphanet:626) |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 | (OMIM:155601) |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 | (OMIM:609048) |
MITF-related melanoma and renal cell carcinoma predisposition syndrome | (Orphanet:293822) |
Melanoma and neural system tumor syndrome | (Orphanet:252206) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |
Xeroderma pigmentosum complementation group C | (Orphanet:276255) |
Xeroderma pigmentosum variant | (Orphanet:90342) |