Abnormality of dentin

Symptom Information:

Symptom ID: HPO:0010299
Synonyms:
Dentine anomaly [Orphanet:12500]
Quality:
Cross references:
Orphanet:12500 "Dentine anomaly" [Orphanet:12500]
Is a (Direct Parents):
HPO         Abnormality of dental structure
Orphanet Abnormality of the teeth
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:
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)