Taurodontia
Symptom Information:
Symptom ID: | HPO:0000679 | ||||||||
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 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) Abnormality of molar(HPO:0011077) Abnormality of molar morphology(HPO:0011070) Abnormality of permanent molar morphology(HPO:0011071) Taurodontia(HPO:0000679) MedDRA: |
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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) |