Abnormality of dental enamel

Symptom Information:

Symptom ID: HPO:0000682
Synonyms:
Abnormal tooth enamel [HPO:0000682]
Enamel abnormalities [HPO:0000682]
Enamel abnormality [HPO:0000682]
Enamel anomaly [Orphanet:12450]
Abnormal tooth enamel [OMIM:Abnormal tooth enamel]
Enamel abnormalities [OMIM:Enamel abnormalities]
Enamel anomaly [MedDRA:10014576]
Quality:
Cross references:
Orphanet:12450 "Enamel anomaly" [Orphanet:12450]
OMIM: "Abnormal tooth enamel" [OMIM:Abnormal tooth enamel]
OMIM: "Enamel abnormalities" [OMIM:Enamel abnormalities]
UMLS:C0235694 "Enamel anomaly" [Orphanet:12450]
Is a (Direct Parents):
MedDRA Dental surface disorders
HPO         Abnormality of dental structure
Orphanet Abnormality of the teeth
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)
                            Abnormality of dental enamel(HPO:0000682)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Dental surface disorders(MedDRA:10012329)
          Abnormality of dental enamel(HPO:0000682)
Database Frequency: 102 / 7739
Resource:

All diseases associated with this symptom:

17q11.2 microduplication syndrome (Orphanet:139474)
22q11.2 deletion syndrome (Orphanet:567)
3M syndrome (Orphanet:2616)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
AREDYLD syndrome (Orphanet:1133)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Amelo-cerebro-hypohidrotic syndrome (Orphanet:1946)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Amelogenesis imperfecta - nephrocalcinosis (Orphanet:1031)
Amelogenesis imperfecta and gingival hyperplasia syndrome (Orphanet:171836)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 4 (OMIM:615982)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CHARGE syndrome (Orphanet:138)
CODAS syndrome (Orphanet:1458)
Cenani-Lenz syndrome (Orphanet:3258)
Childhood-onset hypophosphatasia (Orphanet:247667)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Costello syndrome (Orphanet:3071)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Dental ankylosis (Orphanet:1077)
Dysosteosclerosis (Orphanet:1782)
Dystrophic epidermolysis bullosa (Orphanet:303)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Familial isolated hypoparathyroidism (Orphanet:2238)
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland (Orphanet:2239)
Focal dermal hypoplasia (Orphanet:2092)
Fukuda-Miyanomae-Nakata syndrome (Orphanet:2060)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Gorlin syndrome (Orphanet:377)
Hall-Riggs syndrome (Orphanet:2107)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypophosphatemic rickets (Orphanet:437)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Incontinentia pigmenti (Orphanet:464)
Jalili syndrome (Orphanet:1873)
Junctional epidermolysis bullosa (Orphanet:305)
KBG syndrome (Orphanet:2332)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Kindler syndrome (Orphanet:2908)
Koolen-De Vries syndrome (Orphanet:96169)
LOC syndrome (Orphanet:2407)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
McCune-Albright syndrome (Orphanet:562)
Microcephalic primordial dwarfism, Toriello type (Orphanet:2643)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mucopolysaccharidosis type 4 (Orphanet:582)
Naegeli-Franceschetti-Jadassohn syndrome (Orphanet:69087)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodentodigital dysplasia (Orphanet:2710)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Osteopenia - myopia - hearing loss - intellectual deficit - facial dysmorphism (Orphanet:91133)
Otodental syndrome (Orphanet:2791)
Pfeiffer-Palm-Teller syndrome (Orphanet:2871)
Pili torti (Orphanet:2889)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Prader-Willi syndrome (Orphanet:739)
Proteus syndrome (Orphanet:744)
Proximal renal tubular acidosis (Orphanet:47159)
Pseudohypoaldosteronism type 2 (Orphanet:757)
Ramon syndrome (Orphanet:3019)
SCARF syndrome (Orphanet:3134)
SHORT syndrome (Orphanet:3163)
Sanjad-Sakati syndrome (Orphanet:2323)
Scheie syndrome (Orphanet:93474)
Seckel syndrome (Orphanet:808)
Sjögren-Larsson syndrome (Orphanet:816)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Steroid dehydrogenase deficiency - dental anomalies (Orphanet:3196)
Stickler syndrome (Orphanet:828)
Stimmler syndrome (Orphanet:3199)
Stüve-Wiedemann syndrome (Orphanet:3206)
Taurodontism (Orphanet:3289)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Timothy syndrome (Orphanet:65283)
Treacher-Collins syndrome (Orphanet:861)
Tricho-dento-osseous syndrome (Orphanet:3352)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
Trichodysplasia - amelogenesis imperfecta (Orphanet:79129)
Tuberous sclerosis (Orphanet:805)
Usher syndrome (Orphanet:886)
Usher syndrome type 1 (Orphanet:231169)
Usher syndrome type 2 (Orphanet:231178)
Williams syndrome (Orphanet:904)
X-linked hypophosphatemia (Orphanet:89936)
Zlotogora-Ogur syndrome (Orphanet:3253)