Increased number of teeth

Symptom Information:

Symptom ID: HPO:0011069
Synonyms:
Supernumerary teeth [HPO:0011069]
Supernumerary tooth [HPO:0011069]
Supernumerary tooth [Orphanet:12250]
Supernumerary tooth (disorder) [Orphanet:12250]
Supernumerary tooth (body structure) [Orphanet:12250]
Tooth, Supernumerary [Orphanet:12250]
Supernumerary teeth [OMIM:Supernumerary teeth]
Supernumerary teeth/polyodontia [Orphanet:12250]
Supernumerary teeth [Orphanet:12250]
Supernumerary teeth [MedDRA:10042572]
Supernumerary teeth (in some patients) [OMIM:Supernumerary teeth (in some patients)]
Quality:
Cross references:
HPO:0011067 "Mesiodens" [Orphanet:12250]
Orphanet:12250 "Supernumerary teeth/polyodontia" [Orphanet:12250]
OMIM: "Supernumerary teeth" [OMIM:Supernumerary teeth]
OMIM: "Supernumerary teeth (in some patients)" [OMIM:Supernumerary teeth (in some patients)]
UMLS:C0040457 "Tooth, Supernumerary" [Orphanet:12250]
Is a (Direct Parents):
HPO         Abnormal number of teeth
Orphanet Abnormality of the teeth
MedDRA Dental developmental disorders and anomalies
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)
                            Increased number of teeth(HPO:0011069)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Dental developmental disorders and anomalies(MedDRA:10012321)
          Increased number of teeth(HPO:0011069)
Database Frequency: 39 / 7739
Resource:

All diseases associated with this symptom:

APC-related attenuated familial adenomatous polyposis (Orphanet:247806)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis (Orphanet:86818)
Alström syndrome (Orphanet:64)
Attenuated familial adenomatous polyposis (Orphanet:220460)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
Cleidocranial dysplasia (Orphanet:1452)
Craniosynostosis and dental anomalies (Orphanet:284149)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Familial adenomatous polyposis (Orphanet:733)
Gardner syndrome (Orphanet:79665)
Hallermann-Streiff syndrome (Orphanet:2108)
Hennekam syndrome (Orphanet:2136)
IMPACTED TEETH, MULTIPLE (OMIM:308280)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Langer-Giedion syndrome (Orphanet:502)
Nance-Horan syndrome (Orphanet:627)
Nephrogenic diabetes insipidus - intracranial calcification (Orphanet:3145)
OROFACIODIGITAL SYNDROME XIV (OMIM:615948)
Oculofaciocardiodental syndrome (Orphanet:2712)
Opitz G/BBB syndrome (Orphanet:2745)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Otodental syndrome (Orphanet:2791)
Rothmund-Thomson syndrome (Orphanet:2909)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Steroid dehydrogenase deficiency - dental anomalies (Orphanet:3196)
TEETH, SUPERNUMERARY (OMIM:187100)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
Tricho-retino-dento-digital syndrome (Orphanet:1264)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Turcot syndrome with polyposis (Orphanet:99818)
Zimmermann-Laband syndrome (Orphanet:3473)
Zunich-Kaye syndrome (Orphanet:3474)