Abnormality of dental enamel
Symptom Information:
Symptom ID: | HPO:0000682 | |||||||
Synonyms: |
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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) 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) |
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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) |