Carious teeth
Symptom Information:
Symptom ID: | HPO:0000670 | ||||||||||||||||||||||||||||||
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) Abnormality of dental structure(HPO:0011061) Carious teeth(HPO:0000670) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Dental and periodontal infections and inflammations(MedDRA:10012325) Carious teeth(HPO:0000670) |
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Database Frequency: | 145 / 7739 | ||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
49,XXXXY syndrome | (Orphanet:96264) |
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5 | (OMIM:615887) |
ANE syndrome | (Orphanet:157954) |
APC-related attenuated familial adenomatous polyposis | (Orphanet:247806) |
Adult hypophosphatasia | (Orphanet:247676) |
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
Alström syndrome | (Orphanet:64) |
Anonychia - microcephaly | (Orphanet:1094) |
Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
Aplasia of lacrimal and salivary glands | (Orphanet:86815) |
Aspartylglucosaminuria | (Orphanet:93) |
Attenuated familial adenomatous polyposis | (Orphanet:220460) |
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
Autosomal recessive cutis laxa type 2, classic type | (Orphanet:357074) |
Autosomal recessive cutis laxa type 2A | (Orphanet:357058) |
Autosomal recessive epidermolysis bullosa simplex | (Orphanet:89838) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
Blepharo-cheilo-odontic syndrome | (Orphanet:1997) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
CRANIOMETADIAPHYSEAL DYSPLASIA | (OMIM:269300) |
Calvarial doughnut lesions - bone fragility | (Orphanet:85192) |
Camurati-Engelmann disease | (Orphanet:1328) |
Childhood-onset hypophosphatasia | (Orphanet:247667) |
Cleft palate - short stature - vertebral anomalies | (Orphanet:2015) |
Cockayne syndrome | (Orphanet:191) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
Craniometadiaphyseal dysplasia, wormian bone type | (Orphanet:85184) |
Cutis laxa | (Orphanet:209) |
Cyclic neutropenia | (Orphanet:2686) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 | (OMIM:127550) |
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 | (OMIM:224230) |
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type | (Orphanet:363444) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Distal trisomy 18q | (Orphanet:1716) |
Dubowitz syndrome | (Orphanet:235) |
Dyskeratosis congenita | (Orphanet:1775) |
Dysostosis, Stanescu type | (Orphanet:1798) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET | (OMIM:129540) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
EEM syndrome | (Orphanet:1897) |
Ectodermal dysplasia - sensorineural deafness | (Orphanet:1883) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Familial adenomatous polyposis | (Orphanet:733) |
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome | (Orphanet:313846) |
Familial osteodysplasia, Anderson type | (Orphanet:2769) |
Flynn-Aird syndrome | (Orphanet:2047) |
Gardner syndrome | (Orphanet:79665) |
Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
Generalized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:79402) |
Gorlin syndrome | (Orphanet:377) |
Hereditary acrokeratotic poikiloderma of Kindler-Weary | (Orphanet:306539) |
Hermansky-Pudlak syndrome with neutropenia | (Orphanet:183678) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome | (Orphanet:363523) |
Hypomaturation amelogenesis imperfecta | (Orphanet:100033) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Jalili syndrome | (Orphanet:1873) |
Junctional epidermolysis bullosa inversa | (Orphanet:79405) |
Junctional epidermolysis bullosa, Herlitz type | (Orphanet:79404) |
Junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:89840) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KID syndrome | (Orphanet:477) |
Kenny-Caffey syndrome | (Orphanet:2333) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Kindler syndrome | (Orphanet:2908) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Lichstenstein syndrome | (Orphanet:2390) |
Localized junctional epidermolysis bullosa, non-Herlitz type | (Orphanet:251393) |
MELAS | (Orphanet:550) |
McCune-Albright syndrome | (Orphanet:562) |
Metaphyseal chondrodysplasia, Spahr type | (Orphanet:2501) |
Monosomy 18p | (Orphanet:1598) |
Mucopolysaccharidosis type 4 | (Orphanet:582) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
Naegeli-Franceschetti-Jadassohn syndrome | (Orphanet:69087) |
Nephrogenic diabetes insipidus - intracranial calcification | (Orphanet:3145) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Night blindness - skeletal anomalies - dysmorphism | (Orphanet:1390) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
OCULODENTODIGITAL DYSPLASIA | (OMIM:164200) |
OSLAM syndrome | (Orphanet:2760) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1 | (OMIM:259700) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 | (OMIM:259710) |
OTOFACIOCERVICAL SYNDROME 2 | (OMIM:615560) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculotrichodysplasia | (Orphanet:2718) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteopetrosis | (Orphanet:2781) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
Pachyonychia congenita | (Orphanet:2309) |
Pancreatic insufficiency - anemia - hyperostosis | (Orphanet:199337) |
Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
Prader-Willi syndrome | (Orphanet:739) |
Prolidase deficiency | (Orphanet:742) |
Proteus syndrome | (Orphanet:744) |
Pycnodysostosis | (Orphanet:763) |
Pyle disease | (Orphanet:3005) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency | (Orphanet:353284) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Scheie syndrome | (Orphanet:93474) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Singleton-Merten dysplasia | (Orphanet:85191) |
Stern-Lubinsky-Durrie syndrome | (Orphanet:3194) |
Suarez-Stickler syndrome | (Orphanet:166277) |
Systemic sclerosis | (Orphanet:90291) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Tricho-dento-osseous syndrome | (Orphanet:3352) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Trisomy 4p | (Orphanet:1738) |
Turcot syndrome with polyposis | (Orphanet:99818) |
Usher syndrome | (Orphanet:886) |
Usher syndrome type 2 | (Orphanet:231178) |
Williams syndrome | (Orphanet:904) |
Wrinkly skin syndrome | (Orphanet:2834) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |