Taurodontia

Symptom Information:

Symptom ID: HPO:0000679
Synonyms:
Taurodontism [HPO:0000679]
Taurodontism (disorder) [Orphanet:12100]
Taurodontism [Orphanet:12100]
Taurodontia [OMIM:Taurodontia]
Taurodontism [OMIM:Taurodontism]
Taurodontia [Orphanet:12100]
Taurodontism (in some patients) [OMIM:Taurodontism (in some patients)]
Taurodontism (reported in 1 patient) [OMIM:Taurodontism (reported in 1 patient)]
Quality:
Cross references:
Orphanet:12100 "Taurodontia" [Orphanet:12100]
OMIM: "Taurodontia" [OMIM:Taurodontia]
OMIM: "Taurodontism" [OMIM:Taurodontism]
OMIM: "Taurodontism (in some patients)" [OMIM:Taurodontism (in some patients)]
OMIM: "Taurodontism (reported in 1 patient)" [OMIM:Taurodontism (reported in 1 patient)]
UMLS:C1848911 "Taurodontia" [HPO:0000679]
UMLS:C0266039 "Taurodontism" [Orphanet:12100]
Is a (Direct Parents):
HPO         Abnormality of the dental pulp
Orphanet Abnormality of the teeth
HPO         Abnormality of permanent molar morphology
HPO         Abnormality of the dental root
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 molar(HPO:0011077)
                            Abnormality of molar morphology(HPO:0011070)
                               Abnormality of permanent molar morphology(HPO:0011071)
                                  Taurodontia(HPO:0000679)
                         Abnormality of dental structure(HPO:0011061)
                            Abnormality of the dental pulp(HPO:0006479)
                               Taurodontia(HPO:0000679)
                         Abnormality of dental morphology(HPO:0006482)
                            Abnormality of molar morphology(HPO:0011070)
                               Abnormality of permanent molar morphology(HPO:0011071)
                                  Taurodontia(HPO:0000679)
                            Abnormality of the dental root(HPO:0006486)
                               Taurodontia(HPO:0000679)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
AMELOGENESIS IMPERFECTA, TYPE IA (OMIM:104530)
Ackerman syndrome (Orphanet:2561)
Atypical dentin dysplasia due to SMOC2 deficiency (Orphanet:314721)
CEREBELLOFACIODENTAL SYNDROME (OMIM:616202)
Cranioectodermal dysplasia (Orphanet:1515)
Deaf blind hypopigmentation syndrome, Yemenite type (Orphanet:3214)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
EEC syndrome (Orphanet:1896)
Hypercalcemic tumoral calcinosis (Orphanet:306661)
Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism (Orphanet:100034)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
MOMO syndrome (Orphanet:2563)
Mucopolysaccharidosis type 2 (Orphanet:580)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodentodigital dysplasia (Orphanet:2710)
Oculootodental syndrome (Orphanet:99806)
Otodental syndrome (Orphanet:2791)
Smith-Magenis syndrome (Orphanet:819)
TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS (OMIM:313490)
Taurodontia - absent teeth - sparse hair (Orphanet:2731)
Taurodontism (Orphanet:3289)
Tricho-dento-osseous syndrome (Orphanet:3352)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)