Melanoma
Symptom Information:
Symptom ID: | HPO:0002861 | ||||||||||||||||||||||||||||||||||||||||
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) Neoplasm(HPO:0002664) Neoplasm by histology(HPO:0011792) Melanoma(HPO:0002861) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin neoplasms malignant and unspecified(MedDRA:10040900) Melanoma(HPO:0002861) |
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Database Frequency: | 18 / 7739 | ||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Cowden syndrome | (Orphanet:201) |
Familial melanoma | (Orphanet:618) |
Large congenital melanocytic nevus | (Orphanet:626) |
Li-Fraumeni syndrome | (Orphanet:524) |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 1 | (OMIM:155600) |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2 | (OMIM:155601) |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3 | (OMIM:609048) |
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9 | (OMIM:615134) |
Melanoma and neural system tumor syndrome | (Orphanet:252206) |
Melanoma-pancreatic cancer syndrome | (Orphanet:51013) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Neurocutaneous melanocytosis | (Orphanet:2481) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Oculocutaneous albinism type 2 | (Orphanet:79432) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Xeroderma pigmentosum | (Orphanet:910) |
Xeroderma pigmentosum complementation group B | (Orphanet:276252) |
Xeroderma pigmentosum complementation group E | (Orphanet:276261) |