Periapical radiolucency
Symptom Information:
Symptom ID: | HPO:0000700 | ||
Synonyms: |
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Quality: | |||
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) Abnormality of the teeth(HPO:0000164) Periapical radiolucency(HPO:0000700) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Atypical dentin dysplasia due to SMOC2 deficiency | (Orphanet:314721) |
Dentinogenesis imperfecta type 3 | (Orphanet:166265) |