Papillary thyroid carcinoma

Symptom Information:

Symptom ID: HPO:0002895
Synonyms:
Papillary carcinoma of thyroid [HPO:0002895]
Thyroid papillary carcinoma [HPO:0002895]
Papillary carcinoma of thyroid [OMIM:Papillary carcinoma of thyroid]
Papillary thyroid carcinoma [OMIM:Papillary thyroid carcinoma]
Thyroid papillary carcinoma [OMIM:Thyroid papillary carcinoma]
Papillary thyroid carcinoma (rare) [OMIM:Papillary thyroid carcinoma (rare)]
Quality:
Cross references:
OMIM: "Papillary carcinoma of thyroid" [OMIM:Papillary carcinoma of thyroid]
OMIM: "Papillary thyroid carcinoma" [OMIM:Papillary thyroid carcinoma]
OMIM: "Thyroid papillary carcinoma" [OMIM:Thyroid papillary carcinoma]
OMIM: "Papillary thyroid carcinoma (rare)" [OMIM:Papillary thyroid carcinoma (rare)]
Is a (Direct Parents):
HPO         Thyroid carcinoma
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          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 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(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)
MedDRA:
Database Frequency: 10 / 7739
Resource:

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)