Conical tooth
Symptom Information:
Symptom ID: | HPO:0000698 | |||||||
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 morphology(HPO:0006482) Conical tooth(HPO:0000698) MedDRA: |
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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) |