Increased number of teeth
Symptom Information:
Symptom ID: | HPO:0011069 | |||||||||||
Synonyms: |
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Quality: | ||||||||||||
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) 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) |
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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) |