Oligodontia
Symptom Information:
Symptom ID: | HPO:0000677 | ||||||||||||||
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) Abnormal number of teeth(HPO:0006483) Reduced number of teeth(HPO:0009804) Oligodontia(HPO:0000677) MedDRA: |
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Database Frequency: | 41 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
2q32q33 microdeletion syndrome | (Orphanet:251019) |
ADULT syndrome | (Orphanet:978) |
AGONADISM, 46,XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDEDBONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS | (OMIM:600908) |
AXENFELD-RIEGER SYNDROME, TYPE 1 | (OMIM:180500) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
BRACHYDACTYLY, TYPE E2 | (OMIM:613382) |
Bloom syndrome | (Orphanet:125) |
Brachyolmia-amelogenesis imperfecta syndrome | (Orphanet:2899) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Cherubism | (Orphanet:184) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
Deafness - oligodontia | (Orphanet:3230) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Dysosteosclerosis | (Orphanet:1782) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia with natal teeth, Turnpenny type | (Orphanet:69083) |
Endosteal sclerosis - cerebellar hypoplasia | (Orphanet:85186) |
Focal dermal hypoplasia | (Orphanet:2092) |
Hennekam syndrome | (Orphanet:2136) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
KBG syndrome | (Orphanet:2332) |
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM | (OMIM:614381) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Mandibulofacial dysostosis - macroblepharon - macrostomia | (Orphanet:357158) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Odontoleukodystrophy | (Orphanet:77295) |
Oligodontia - cancer predisposition syndrome | (Orphanet:300576) |
Pseudoaminopterin syndrome | (Orphanet:221120) |
Spondyloepimetaphyseal dysplasia - abnormal dentition | (Orphanet:168451) |
TOOTH AGENESIS, SELECTIVE, 3 | (OMIM:604625) |
TOOTH AGENESIS, SELECTIVE, 6 | (OMIM:613097) |
TOOTH AGENESIS, SELECTIVE, X-LINKED, 1 | (OMIM:313500) |
Taurodontia - absent teeth - sparse hair | (Orphanet:2731) |
Tricho-oculo-dermo-vertebral syndrome | (Orphanet:3354) |
Tricho-retino-dento-digital syndrome | (Orphanet:1264) |
Wilson-Turner syndrome | (Orphanet:3459) |
Zechi-Ceide syndrome | (Orphanet:217017) |