Abnormal pigmentation of the oral mucosa
Symptom Information:
Symptom ID: | HPO:0100669 | ||||
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) 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) Abnormal pigmentation of the oral mucosa(HPO:0100669) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Carney complex | (Orphanet:1359) |
Dyschromatosis universalis hereditaria 1 | (OMIM:127500) |
Dyschromatosis universalis hereditaria 2 | (OMIM:612715) |
Dyschromatosis universalis hereditaris 3 | (OMIM:615402) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
LOC syndrome | (Orphanet:2407) |
Peutz-Jeghers syndrome | (Orphanet:2869) |