Fibroma
Symptom Information:
Symptom ID: | HPO:0010614 | ||||||
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) Fibrous tissue neoplasm(HPO:0012316) Fibroma(HPO:0010614) MedDRA: Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104) Miscellaneous and site unspecified neoplasms benign(MedDRA:10027656) Neoplasms benign site unspecified NEC(MedDRA:10029106) Fibroma(HPO:0010614) |
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Database Frequency: | 10 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
APC-related attenuated familial adenomatous polyposis | (Orphanet:247806) |
Familial adenomatous polyposis | (Orphanet:733) |
Gardner syndrome | (Orphanet:79665) |
Infantile myofibromatosis | (Orphanet:2591) |
Melanoma and neural system tumor syndrome | (Orphanet:252206) |
Neurofibromatosis type 1 | (Orphanet:636) |
Neurofibromatosis type 2 | (Orphanet:637) |
Terminal osseous dysplasia - pigmentary defects | (Orphanet:88630) |
Tuberous sclerosis | (Orphanet:805) |
Turcot syndrome with polyposis | (Orphanet:99818) |