Abnormality of the teeth

Symptom Information:

Symptom ID: HPO:0000164
Synonyms:
Abnormal dentition [HPO:0000164]
Abnormal teeth [HPO:0000164]
Dental abnormalities [HPO:0000164]
Dental abnormality [HPO:0000164]
Dental anomalies [HPO:0000164]
Tooth abnormalities [HPO:0000164]
Tooth anomaly [Orphanet:12000]
Tooth malformation (disorder) [Orphanet:12000]
Tooth Abnormalities [Orphanet:12000]
Abnormal dentition [OMIM:Abnormal dentition]
Abnormal teeth [OMIM:Abnormal teeth]
Dental abnormalities [OMIM:Dental abnormalities]
Dental anomalies [OMIM:Dental anomalies]
Tooth abnormalities [OMIM:Tooth abnormalities]
Anomalies of teeth and dentition [Orphanet:12000]
Tooth malformation [Orphanet:12000]
Tooth malformation [MedDRA:10044046]
Abnormalities of size and form of teeth [MedDRA:10044046]
Anomalies of dental arch relationship [MedDRA:10044046]
Anomalies of tooth position [MedDRA:10044046]
Anomaly of dental arch [MedDRA:10044046]
Anomaly teeth [MedDRA:10044046]
Hutchinson's teeth [MedDRA:10044046]
Malformation tooth [MedDRA:10044046]
Abnormal dentition (classic features, NOLA3 patient) [OMIM:Abnormal dentition (classic features, NOLA3 patient)]
Abnormal dentition (in some patients) [OMIM:Abnormal dentition (in some patients)]
Abnormal teeth (in some patients) [OMIM:Abnormal teeth (in some patients)]
Quality:
Cross references:
Orphanet:12000 "Anomalies of teeth and dentition" [Orphanet:12000]
OMIM: "Abnormal dentition" [OMIM:Abnormal dentition]
OMIM: "Abnormal teeth" [OMIM:Abnormal teeth]
OMIM: "Dental abnormalities" [OMIM:Dental abnormalities]
OMIM: "Dental anomalies" [OMIM:Dental anomalies]
OMIM: "Tooth abnormalities" [OMIM:Tooth abnormalities]
OMIM: "Abnormal dentition (classic features, NOLA3 patient)" [OMIM:Abnormal dentition (classic features, NOLA3 patient)]
OMIM: "Abnormal dentition (in some patients)" [OMIM:Abnormal dentition (in some patients)]
OMIM: "Abnormal teeth (in some patients)" [OMIM:Abnormal teeth (in some patients)]
UMLS:C0040427 "Tooth Abnormalities" [Orphanet:12000]
Is a (Direct Parents):
HPO         Irregular dentition
MedDRA Dental developmental disorders and anomalies
HPO         Abnormality of the oral cavity
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)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Dental developmental disorders and anomalies(MedDRA:10012321)
          Abnormality of the teeth(HPO:0000164)
Database Frequency: 291 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microduplication syndrome (Orphanet:276422)
15q14 microdeletion syndrome (Orphanet:261190)
17q21.31 microduplication syndrome (Orphanet:217340)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
22q11.2 deletion syndrome (Orphanet:567)
3q29 microdeletion syndrome (Orphanet:65286)
3q29 microduplication (Orphanet:251038)
4q21 microdeletion syndrome (Orphanet:238750)
6q16 deletion syndrome (Orphanet:171829)
8q21.11 microdeletion syndrome (Orphanet:284160)
8q22.1 microdeletion syndrome (Orphanet:178303)
ADULT syndrome (Orphanet:978)
AMELOGENIN, Y-CHROMOSOMAL (OMIM:410000)
ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS (OMIM:206600)
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
AREDYLD syndrome (Orphanet:1133)
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:615952)
Aarskog-Scott syndrome (Orphanet:915)
Achondroplasia (Orphanet:15)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Acrofacial dysostosis, Weyers type (Orphanet:952)
Acromegaly (Orphanet:963)
Acroosteolysis, dominant type (Orphanet:955)
Albers-Schönberg osteopetrosis (Orphanet:53)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Alpha-mannosidosis (Orphanet:61)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alström syndrome (Orphanet:64)
Angel-shaped phalango-epiphyseal dysplasia (Orphanet:63442)
Angelman syndrome (Orphanet:72)
Aniridia (Orphanet:77)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Anonychia - microcephaly (Orphanet:1094)
Aspartylglucosaminuria (Orphanet:93)
Ataxia - photosensitivity - short stature (Orphanet:1184)
Atkin-Flaitz syndrome (Orphanet:1193)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal dominant hypophosphatemic rickets (Orphanet:89937)
Autosomal recessive distal osteolysis syndrome (Orphanet:2776)
Autosomal recessive epidermolysis bullosa simplex (Orphanet:89838)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Bangstad syndrome (Orphanet:1227)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 8 (OMIM:615985)
Bardet-Biedl syndrome 9 (OMIM:615986)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Beta-thalassemia major (Orphanet:231214)
Blepharoptosis - cleft palate - ectrodactyly - dental anomalies (Orphanet:1258)
Branchio-oculo-facial syndrome (Orphanet:1297)
Brittle cornea syndrome (Orphanet:90354)
Buschke-Ollendorff syndrome (Orphanet:1306)
Böök syndrome (Orphanet:1262)
CANINE TEETH, ABSENCE OF UPPER PERMANENT (OMIM:114600)
CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH (OMIM:114700)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
CEDNIK syndrome (Orphanet:66631)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiospondylocarpofacial syndrome (Orphanet:3238)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cherubism (Orphanet:184)
Classical homocystinuria (Orphanet:394)
Cleidocranial dysplasia (Orphanet:1452)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Cohen syndrome (Orphanet:193)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Congenital pseudoarthrosis of clavicle (Orphanet:66630)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
Cowden syndrome (Orphanet:201)
Cranioectodermal dysplasia (Orphanet:1515)
Craniofrontonasal dysplasia (Orphanet:1520)
Cryptorchidism - arachnodactyly - intellectual deficit (Orphanet:1548)
DENS EVAGINATUS (OMIM:125280)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Deafness-craniofacial syndrome (Orphanet:3241)
Dental ankylosis (Orphanet:1077)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Dermo-odonto dysplasia (Orphanet:1660)
Distal monosomy 9p (Orphanet:1642)
Distal trisomy 18q (Orphanet:1716)
Down syndrome (Orphanet:870)
Dubowitz syndrome (Orphanet:235)
Dyschondrosteosis - nephritis (Orphanet:1765)
Dyskeratosis congenita (Orphanet:1775)
Dysostosis, Stanescu type (Orphanet:1798)
Dystrophic epidermolysis bullosa (Orphanet:303)
ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE (OMIM:129810)
EEM syndrome (Orphanet:1897)
ERYTHEMA OF ACRAL REGIONS (OMIM:227000)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Ellis Van Creveld syndrome (Orphanet:289)
Enthesitis-related arthritis (Orphanet:85438)
Eosinophilic granuloma (Orphanet:99871)
Epilepsy telangiectasia (Orphanet:1951)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Familial osteodysplasia, Anderson type (Orphanet:2769)
Flynn-Aird syndrome (Orphanet:2047)
Focal dermal hypoplasia (Orphanet:2092)
Fraser syndrome (Orphanet:2052)
Freeman-Sheldon syndrome (Orphanet:2053)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Fucosidosis (Orphanet:349)
Fused mandibular incisors (Orphanet:2287)
GAPO syndrome (Orphanet:2067)
Galloway-Mowat syndrome (Orphanet:2065)
Generalized junctional epidermolysis bullosa, non-Herlitz type (Orphanet:79402)
Gingival fibromatosis-hypertrichosis syndrome (Orphanet:2026)
Gorlin syndrome (Orphanet:377)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE (OMIM:240000)
HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA (OMIM:615266)
HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA (OMIM:615267)
HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA (OMIM:615269)
Hallermann-Streiff syndrome (Orphanet:2108)
Harrod syndrome (Orphanet:2115)
Heart-hand syndrome type 2 (Orphanet:1350)
Hemihypertrophy (Orphanet:2128)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypertrichosis lanuginosa congenita (Orphanet:2222)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Hypomyelination - hypogonadotropic hypogonadism - hypodontia (Orphanet:88637)
Hypophosphatasia (Orphanet:436)
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism (Orphanet:2250)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Hypotrichosis with juvenile macular degeneration (Orphanet:1573)
Ichthyosis - intellectual deficit - dwarfism - renal impairment (Orphanet:2278)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
Insulin-resistance syndrome type A (Orphanet:2297)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome (Orphanet:363611)
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome (Orphanet:369837)
Johanson-Blizzard syndrome (Orphanet:2315)
Junctional epidermolysis bullosa (Orphanet:305)
Juvenile Paget disease (Orphanet:2801)
Juvenile rheumatoid factor-negative polyarthritis (Orphanet:85408)
Juvenile rheumatoid factor-positive polyarthritis (Orphanet:85435)
KABUKI SYNDROME 2 (OMIM:300867)
KBG syndrome (Orphanet:2332)
KID syndrome (Orphanet:477)
Kabuki syndrome (Orphanet:2322)
Koolen-De Vries syndrome (Orphanet:96169)
LOC syndrome (Orphanet:2407)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Lamellar ichthyosis (Orphanet:313)
Langer-Giedion syndrome (Orphanet:502)
Late-onset localized junctional epidermolysis bullosa - intellectual deficit (Orphanet:231556)
Lateral meningocele syndrome (Orphanet:2789)
Legg-Calvé-Perthes disease (Orphanet:2380)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lethal restrictive dermopathy (Orphanet:1662)
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY (OMIM:606369)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 (OMIM:616268)
MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES (OMIM:251700)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Marfan syndrome (Orphanet:558)
Marshall syndrome (Orphanet:560)
McCune-Albright syndrome (Orphanet:562)
McDonough syndrome (Orphanet:2471)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Microphthalmia, Lenz type (Orphanet:568)
Monilethrix (Orphanet:573)
Monosomy 18p (Orphanet:1598)
Monosomy 22q13 (Orphanet:48652)
Monosomy 9p (Orphanet:261112)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 4 (Orphanet:582)
Multiple osteochondromas (Orphanet:321)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Nance-Horan syndrome (Orphanet:627)
Non-distal trisomy 13q (Orphanet:1702)
OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIANBONES, BUT WITHOUT FRACTURES (OMIM:166230)
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 (OMIM:259710)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodental syndrome, Rutherfurd type (Orphanet:2709)
Oculofaciocardiodental syndrome (Orphanet:2712)
Oculomaxillofacial dysostosis (Orphanet:1794)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Odontomicronychial dysplasia (Orphanet:1811)
Odontotrichomelic syndrome (Orphanet:2723)
Oro-mandibular-limb hypogenesis syndrome (Orphanet:2749)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 3 (Orphanet:2752)
Orofaciodigital syndrome type 9 (Orphanet:141007)
Osteogenesis imperfecta (Orphanet:666)
Osteopetrosis (Orphanet:2781)
Otopalatodigital syndrome (Orphanet:669)
PARAMOLAR TUBERCLE OF BOLK (OMIM:168200)
PELGER-HUET ANOMALY (OMIM:169400)
PERMANENT MOLARS, SECONDARY RETENTION OF (OMIM:157950)
PREMATURE OVARIAN FAILURE 2B (OMIM:300604)
Pachyonychia congenita (Orphanet:2309)
Papillon-Lefèvre syndrome (Orphanet:678)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Peters anomaly (Orphanet:708)
Pili torti (Orphanet:2889)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Pitt-Hopkins syndrome (Orphanet:2896)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Pseudohypoaldosteronism type 2 (Orphanet:757)
Pseudoprogeria syndrome (Orphanet:2985)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
Pycnodysostosis (Orphanet:763)
Rabson-Mendenhall syndrome (Orphanet:769)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
Ramon syndrome (Orphanet:3019)
Recombinant 8 syndrome (Orphanet:96167)
Rett syndrome (Orphanet:778)
Rhizomelic chondrodysplasia punctata (Orphanet:177)
Rieger anomaly (Orphanet:91483)
Robin sequence - oligodactyly (Orphanet:3104)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 1 (Orphanet:221008)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
Rubinstein-Taybi syndrome (Orphanet:783)
Ruvalcaba syndrome (Orphanet:3121)
SCARF syndrome (Orphanet:3134)
SHORT syndrome (Orphanet:3163)
SPLIT LOWER LIP (OMIM:183400)
Sanjad-Sakati syndrome (Orphanet:2323)
Say-Barber-Miller syndrome (Orphanet:3132)
Scalp-ear-nipple syndrome (Orphanet:2036)
Scheie syndrome (Orphanet:93474)
Schwartz-Jampel syndrome (Orphanet:800)
Severe combined immunodeficiency (Orphanet:183660)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Skeletal dysplasia - epilepsy - short stature (Orphanet:1858)
Sparse hair - short stature - skin anomalies (Orphanet:79132)
Splenogonadal fusion - limb defects - micrognathia (Orphanet:2063)
Spondyloenchondrodysplasia (Orphanet:1855)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Stüve-Wiedemann syndrome (Orphanet:3206)
Syndromic X-linked intellectual deficit 7 (Orphanet:85274)
Syngnathia multiple anomalies (Orphanet:3262)
Synostosis - microcephaly - scoliosis (Orphanet:3268)
TEETH, FUSED (OMIM:273000)
TEETH, ODD SHAPES OFLOBODONTIA, INCLUDED (OMIM:187000)
TOOTH SIZE (OMIM:314240)
Tetrasomy X (Orphanet:9)
Timothy syndrome (Orphanet:65283)
Treacher-Collins syndrome (Orphanet:861)
Tricho-odonto-onychodysplasia - dominant syndactyly (Orphanet:3357)
Tricho-retino-dento-digital syndrome (Orphanet:1264)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trisomy 13 (Orphanet:3378)
Trisomy 20p (Orphanet:261318)
Trisomy 4p (Orphanet:1738)
Trisomy 9p (Orphanet:236)
Tumoral calcinosis (Orphanet:53715)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Ulnar-mammary syndrome (Orphanet:3138)
Velo-facial-skeletal syndrome (Orphanet:3424)
Williams syndrome (Orphanet:904)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked hypophosphatemia (Orphanet:89936)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
Xeroderma pigmentosum (Orphanet:910)
Zlotogora-Ogur syndrome (Orphanet:3253)
Zunich-Kaye syndrome (Orphanet:3474)