Conical tooth

Symptom Information:

Symptom ID: HPO:0000698
Synonyms:
Conical teeth [HPO:0000698]
Peg shaped teeth [HPO:0000698]
Peg tooth [HPO:0000698]
Peg-shaped teeth [HPO:0000698]
Conical teeth [OMIM:Conical teeth]
Peg-shaped teeth [OMIM:Peg-shaped teeth]
Conical teeth (permanent teeth) [OMIM:Conical teeth (permanent teeth)]
Quality:
Cross references:
OMIM: "Conical teeth" [OMIM:Conical teeth]
OMIM: "Peg-shaped teeth" [OMIM:Peg-shaped teeth]
OMIM: "Conical teeth (permanent teeth)" [OMIM:Conical teeth (permanent teeth)]
Is a (Direct Parents):
HPO         Abnormality of dental morphology
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 morphology(HPO:0006482)
                            Conical tooth(HPO:0000698)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

2q32q33 microdeletion syndrome (Orphanet:251019)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Deafness - onychodystrophy (Orphanet:3231)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT (OMIM:612132)
Ectodermal dysplasia - syndactyly syndrome (Orphanet:247820)
Hurler syndrome (Orphanet:93473)
Mucopolysaccharidosis type 2 (Orphanet:580)
Postaxial acrofacial dysostosis (Orphanet:246)
RAPP-HODGKIN SYNDROME (OMIM:129400)
Trichodental syndrome (Orphanet:3351)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)