Hypodontia
Symptom Information:
Symptom ID: | HPO:0000668 | |||||||||||
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) Hypodontia(HPO:0000668) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Agenesis of permanent teeth(HPO:0006349) Hypodontia(HPO:0000668) |
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Database Frequency: | 81 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
AARSKOG-SCOTT SYNDROME | (OMIM:305400) |
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
ADULT syndrome | (Orphanet:978) |
AGONADISM, 46,XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDEDBONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS | (OMIM:600908) |
ANE syndrome | (Orphanet:157954) |
AREDYLD syndrome | (Orphanet:1133) |
AXENFELD-RIEGER SYNDROME, TYPE 1 | (OMIM:180500) |
AXENFELD-RIEGER SYNDROME, TYPE 2 | (OMIM:601499) |
AXENFELD-RIEGER SYNDROME, TYPE 3 | (OMIM:602482) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Anauxetic dysplasia | (Orphanet:93347) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal dominant hypohidrotic ectodermal dysplasia | (Orphanet:1810) |
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
Axenfeld-Rieger syndrome | (Orphanet:782) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
Bardet-Biedl syndrome | (Orphanet:110) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
Bloom syndrome | (Orphanet:125) |
Böök syndrome | (Orphanet:1262) |
Coffin-Lowry syndrome | (Orphanet:192) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Craniofacial dysplasia-osteopenia syndrome | (Orphanet:314555) |
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT | (OMIM:129490) |
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE | (OMIM:224900) |
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT | (OMIM:612132) |
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME | (OMIM:616029) |
Ectodermal dysplasia with natal teeth, Turnpenny type | (Orphanet:69083) |
Ectodermal dysplasia, Berlin type | (Orphanet:1816) |
Ectodermal dysplasia, tricho-odonto-onychial type | (Orphanet:1818) |
Ehlers-Danlos syndrome, dermatosparaxis type | (Orphanet:1901) |
Ehlers-Danlos syndrome, spondylocheirodysplastic type | (Orphanet:157965) |
Ellis Van Creveld syndrome | (Orphanet:289) |
FAILURE OF TOOTH ERUPTION, PRIMARY | (OMIM:125350) |
Faciocardiorenal syndrome | (Orphanet:1973) |
Filippi syndrome | (Orphanet:3255) |
Focal dermal hypoplasia | (Orphanet:2092) |
Generalized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:79402) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2 | (OMIM:300640) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Incontinentia pigmenti | (Orphanet:464) |
Isolated congenital hypoglossia/aglossia | (Orphanet:141152) |
Junctional epidermolysis bullosa inversa | (Orphanet:79405) |
Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
KABUKI SYNDROME 2 | (OMIM:300867) |
LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM | (OMIM:614381) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
Limb-mammary syndrome | (Orphanet:69085) |
Localized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:251393) |
MALPOSITION OF TEETH WITH OR WITHOUT HYPODONTIA/OLIGODONTIA | (OMIM:189490) |
Mulibrey nanism | (Orphanet:2576) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Odontoleukodystrophy | (Orphanet:77295) |
Oligodontia | (Orphanet:99798) |
Otodental syndrome | (Orphanet:2791) |
Pilodental dysplasia - refractive errors | (Orphanet:2892) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Pycnodysostosis | (Orphanet:763) |
RAPP-HODGKIN SYNDROME | (OMIM:129400) |
Rosselli-Gulienetti syndrome | (Orphanet:90339) |
SENER SYNDROME | (OMIM:606156) |
SHORT syndrome | (Orphanet:3163) |
SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA | (OMIM:183500) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
THAI SYMPHALANGISM SYNDROME | (OMIM:608028) |
TOOTH AGENESIS, SELECTIVE, 1 | (OMIM:106600) |
TOOTH AGENESIS, SELECTIVE, X-LINKED, 1 | (OMIM:313500) |
Trichodental syndrome | (Orphanet:3351) |
Ulnar-mammary syndrome | (Orphanet:3138) |
VAN DER WOUDE SYNDROME 1 | (OMIM:119300) |
Van der Woude syndrome | (Orphanet:888) |
Williams syndrome | (Orphanet:904) |
Wilson-Turner syndrome | (Orphanet:3459) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |