Abnormality of the teeth
Symptom Information:
Symptom ID: | HPO:0000164 | |||||||||||||||||||||||||||
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) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Dental and gingival conditions(MedDRA:10044018) Dental developmental disorders and anomalies(MedDRA:10012321) Abnormality of the teeth(HPO:0000164) |
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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) |