Hamartoma
Symptom Information:
| Symptom ID: | HPO:0010566 | ||||
| Synonyms: |
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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) Hamartoma(HPO:0010566) 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) Hamartoma(HPO:0010566) |
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| Database Frequency: | 7 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Branchio-oculo-facial syndrome | (Orphanet:1297) |
| COWDEN SYNDROME 4 | (OMIM:615107) |
| Generalized basaloid follicular hamartoma syndrome | (Orphanet:168632) |
| HAMARTOMA, PRECALCANEAL CONGENITAL FIBROLIPOMATOUS | (OMIM:609808) |
| Hyperparathyroidism - jaw tumor syndrome | (Orphanet:99880) |
| LIP, HAMARTOMATOUS | (OMIM:151640) |
| Orofaciodigital syndrome type 9 | (Orphanet:141007) |