Oligodontia

Symptom Information:

Symptom ID: HPO:0000677
Synonyms:
Partial anodontia [HPO:0000677]
Partial congenital absence of teeth (disorder) [Orphanet:12300]
Hypodontia [HPO:0000677]
Hypodontia [Orphanet:12300]
Oligodontia [OMIM:Oligodontia]
Anodontia/oligodontia/hypodontia [Orphanet:12300]
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.]
Oligodontia (in some patients) [OMIM:Oligodontia (in some patients)]
Oligodontia (reduced number of molars and premolars) [OMIM:Oligodontia (reduced number of molars and premolars)]
Oligodontia (secondary teeth) [OMIM:Oligodontia (secondary teeth)]
Quality:
Cross references:
Orphanet:12300 "Anodontia/oligodontia/hypodontia" [Orphanet:12300]
OMIM: "Oligodontia" [OMIM:Oligodontia]
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.]
OMIM: "Oligodontia (in some patients)" [OMIM:Oligodontia (in some patients)]
OMIM: "Oligodontia (reduced number of molars and premolars)" [OMIM:Oligodontia (reduced number of molars and premolars)]
OMIM: "Oligodontia (secondary teeth)" [OMIM:Oligodontia (secondary teeth)]
UMLS:C0020608 "Hypodontia" [HPO:0000677]
UMLS:C0020608 "Hypodontia" [Orphanet:12300]
Is a (Direct Parents):
HPO         Reduced number of teeth
Orphanet Abnormality of the teeth
Orphanet Hypodontia
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:
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)