Dentinogenesis imperfecta limited to primary teeth
Symptom Information:
Symptom ID: | HPO:0011060 | ||
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) Abnormality of dental structure(HPO:0011061) Abnormality of dentin(HPO:0010299) Dentinogenesis imperfecta(HPO:0000703) Dentinogenesis imperfecta limited to primary teeth(HPO:0011060) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Atypical dentin dysplasia due to SMOC2 deficiency | (Orphanet:314721) |
Dentin dysplasia - sclerotic bones | (Orphanet:99792) |
Dentin dysplasia type II | (Orphanet:99791) |