Hypodontia

Symptom Information:

Symptom ID: HPO:0000668
Synonyms:
Partial congenital absence of teeth (disorder) [Orphanet:12300]
Hypodontia [Orphanet:12300]
Hypodontia [OMIM:Hypodontia]
Anodontia/oligodontia/hypodontia [Orphanet:12300]
Hypodontia [MedDRA:10055001]
Partial anodontia [MedDRA:10055001]
Hypodontia (in some patients) [OMIM:Hypodontia (in some patients)]
Hypodontia (maxillary incisors) [OMIM:Hypodontia (maxillary incisors)]
Hypodontia (rare) [OMIM:Hypodontia (rare)]
Hypodontia (secondary teeth) [OMIM:Hypodontia (secondary teeth)]
Hypodontia. [OMIM:Hypodontia.]
Quality:
Cross references:
Orphanet:12300 "Anodontia/oligodontia/hypodontia" [Orphanet:12300]
OMIM: "Hypodontia" [OMIM:Hypodontia]
OMIM: "Hypodontia (in some patients)" [OMIM:Hypodontia (in some patients)]
OMIM: "Hypodontia (maxillary incisors)" [OMIM:Hypodontia (maxillary incisors)]
OMIM: "Hypodontia (rare)" [OMIM:Hypodontia (rare)]
OMIM: "Hypodontia (secondary teeth)" [OMIM:Hypodontia (secondary teeth)]
OMIM: "Hypodontia." [OMIM:Hypodontia.]
UMLS:C0020608 "Hypodontia" [HPO:0000668]
UMLS:C0020608 "Hypodontia" [Orphanet:12300]
Is a (Direct Parents):
HPO         Reduced number of teeth
MedDRA Agenesis of permanent teeth
Orphanet Abnormality of the teeth
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)
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)