Carious teeth

Symptom Information:

Symptom ID: HPO:0000670
Synonyms:
Caries [HPO:0000670]
Dental caries [HPO:0000670]
Dental decay [HPO:0000670]
Early dental caries [HPO:0000670]
Frequent caries [HPO:0000670]
Dental caries [Orphanet:12650]
Dental caries (disorder) [Orphanet:12650]
Caries (morphologic abnormality) [Orphanet:12650]
Caries [OMIM:Caries]
Carious teeth [OMIM:Carious teeth]
Dental caries [OMIM:Dental caries]
Early dental caries [OMIM:Early dental caries]
Frequent caries [OMIM:Frequent caries]
Multiple caries [Orphanet:12650]
Dental caries [MedDRA:10012318]
Caries dental [MedDRA:10012318]
Cavity [MedDRA:10012318]
Cavity NOS [MedDRA:10012318]
Decay dental [MedDRA:10012318]
Dental caries aggravated [MedDRA:10012318]
Tooth caries [MedDRA:10012318]
Tooth caries aggravated [MedDRA:10012318]
Tooth caries aggravated NOS [MedDRA:10012318]
Tooth caries NOS [MedDRA:10012318]
Tooth decay [MedDRA:10012318]
Tooth cavity [MedDRA:10012318]
Dental decay [MedDRA:10012318]
Dental cavity [MedDRA:10012318]
Dental caries (classic feature) [OMIM:Dental caries (classic feature)]
Dental caries (secondary teeth) [OMIM:Dental caries (secondary teeth)]
Quality:
Cross references:
Orphanet:12650 "Multiple caries" [Orphanet:12650]
OMIM: "Caries" [OMIM:Caries]
OMIM: "Carious teeth" [OMIM:Carious teeth]
OMIM: "Dental caries" [OMIM:Dental caries]
OMIM: "Early dental caries" [OMIM:Early dental caries]
OMIM: "Frequent caries" [OMIM:Frequent caries]
OMIM: "Dental caries (classic feature)" [OMIM:Dental caries (classic feature)]
OMIM: "Dental caries (secondary teeth)" [OMIM:Dental caries (secondary teeth)]
UMLS:C0011334 "Dental caries" [Orphanet:12650]
UMLS:C0333519 "Caries (morphologic abnormality)" [Orphanet:12650]
Is a (Direct Parents):
HPO         Abnormality of dental structure
Orphanet Abnormality of the teeth
MedDRA Dental and periodontal infections and inflammations
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)
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)