Dentinogenesis imperfecta limited to primary teeth

Symptom Information:

Symptom ID: HPO:0011060
Synonyms:
Dentin dysplasia [HPO:0011060]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Dentinogenesis imperfecta
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:
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)