Papillary thyroid carcinoma
Symptom Information:
Symptom ID: | HPO:0002895 | ||||||
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 anatomical site(HPO:0011793) Neoplasm of the endocrine system(HPO:0100568) Neoplasm of the thyroid gland(HPO:0100031) Thyroid carcinoma(HPO:0002890) Papillary thyroid carcinoma(HPO:0002895) Abnormality of the endocrine system(HPO:0000818) Abnormality of the thyroid gland(HPO:0000820) Abnormality of thyroid morphology(HPO:0011772) Neoplasm of the thyroid gland(HPO:0100031) Thyroid carcinoma(HPO:0002890) Papillary thyroid carcinoma(HPO:0002895) Neoplasm of the endocrine system(HPO:0100568) Neoplasm of the thyroid gland(HPO:0100031) Thyroid carcinoma(HPO:0002890) Papillary thyroid carcinoma(HPO:0002895) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||||
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All diseases associated with this symptom:
APC-related attenuated familial adenomatous polyposis | (Orphanet:247806) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Attenuated familial adenomatous polyposis | (Orphanet:220460) |
COWDEN SYNDROME 2 | (OMIM:612359) |
Familial adenomatous polyposis | (Orphanet:733) |
Familial multinodular goiter | (Orphanet:276399) |
Gardner syndrome | (Orphanet:79665) |
THYROID CARCINOMA, PAPILLARY | (OMIM:188550) |
Turcot syndrome with polyposis | (Orphanet:99818) |