Neoplasm of the oral cavity
Symptom Information:
Symptom ID: | HPO:0100649 | ||||||||||||||||||||||||||||||||
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 oral cavity(HPO:0100649) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Abnormality of the oral cavity(HPO:0000163) Neoplasm of the oral cavity(HPO:0100649) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Malignant and unspecified neoplasms gastrointestinal NEC(MedDRA:10017990) Oral cavity neoplasms NEC(MedDRA:10030969) Neoplasm of the oral cavity(HPO:0100649) |
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Database Frequency: | 20 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Gingival fibromatosis-hypertrichosis syndrome | (Orphanet:2026) |
Gorlin syndrome | (Orphanet:377) |
Heart defect - tongue hamartoma - polysyndactyly | (Orphanet:1338) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Lichen planopilaris | (Orphanet:525) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 3 | (Orphanet:2752) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
PTEN hamartoma tumor syndrome | (Orphanet:306498) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
Werner syndrome | (Orphanet:902) |
Xeroderma pigmentosum | (Orphanet:910) |