Neoplasm of the thyroid gland
Symptom Information:
Symptom ID: | HPO:0100031 | ||||
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 anatomical site(HPO:0011793) Neoplasm of the endocrine system(HPO:0100568) Neoplasm of the thyroid gland(HPO:0100031) Abnormality of the endocrine system(HPO:0000818) Neoplasm of the endocrine system(HPO:0100568) Neoplasm of the thyroid gland(HPO:0100031) Abnormality of the thyroid gland(HPO:0000820) Abnormality of thyroid morphology(HPO:0011772) Neoplasm of the thyroid gland(HPO:0100031) MedDRA: |
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Database Frequency: | 15 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Albright hereditary osteodystrophy | (Orphanet:665) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Birt-Hogg-Dube syndrome | (Orphanet:122) |
COWDEN SYNDROME 3 | (OMIM:615106) |
Carney complex | (Orphanet:1359) |
Cowden syndrome | (Orphanet:201) |
Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
Hirschsprung disease | (Orphanet:388) |
McCune-Albright syndrome | (Orphanet:562) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
PTEN hamartoma tumor syndrome | (Orphanet:306498) |
Pendred syndrome | (Orphanet:705) |
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
Werner syndrome | (Orphanet:902) |