Abnormality of dentin
Symptom Information:
Symptom ID: | HPO:0010299 | ||||
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) Abnormality of the teeth(HPO:0000164) Abnormality of dental structure(HPO:0011061) Abnormality of dentin(HPO:0010299) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Cole-Carpenter syndrome | (Orphanet:2050) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Dentin dysplasia | (Orphanet:1653) |
Dentinogenesis imperfecta - short stature - hearing loss - intellectual deficit | (Orphanet:71267) |
Dysostosis, Stanescu type | (Orphanet:1798) |
Goldblatt syndrome | (Orphanet:166272) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Osteogenesis imperfecta | (Orphanet:666) |
Suarez-Stickler syndrome | (Orphanet:166277) |