Hypoplasia of dental enamel

Symptom Information:

Symptom ID: HPO:0006297
Synonyms:
Dental enamel hypoplasia [HPO:0006297]
Enamel dysplasia [HPO:0006297]
Enamel hypoplasia [HPO:0006297]
Thin dental enamel [HPO:0006297]
Dental enamel hypoplasia [OMIM:Dental enamel hypoplasia]
Enamel dysplasia [OMIM:Enamel dysplasia]
Enamel hypoplasia [OMIM:Enamel hypoplasia]
Thin dental enamel [OMIM:Thin dental enamel]
Enamel dysplasia (in some patients) [OMIM:Enamel dysplasia (in some patients)]
Enamel hypoplasia (amelogenesis imperfecta) [OMIM:Enamel hypoplasia (amelogenesis imperfecta)]
Enamel hypoplasia (in one family) [OMIM:Enamel hypoplasia (in one family)]
Quality:
Cross references:
OMIM: "Dental enamel hypoplasia" [OMIM:Dental enamel hypoplasia]
OMIM: "Enamel dysplasia" [OMIM:Enamel dysplasia]
OMIM: "Enamel hypoplasia" [OMIM:Enamel hypoplasia]
OMIM: "Thin dental enamel" [OMIM:Thin dental enamel]
OMIM: "Enamel dysplasia (in some patients)" [OMIM:Enamel dysplasia (in some patients)]
OMIM: "Enamel hypoplasia (amelogenesis imperfecta)" [OMIM:Enamel hypoplasia (amelogenesis imperfecta)]
OMIM: "Enamel hypoplasia (in one family)" [OMIM:Enamel hypoplasia (in one family)]
Is a (Direct Parents):
HPO         Hypoplasia of teeth
HPO         Abnormality of dental enamel
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)
                               Hypoplasia of dental enamel(HPO:0006297)
                            Hypoplasia of teeth(HPO:0000685)
                               Hypoplasia of dental enamel(HPO:0006297)
MedDRA:
Database Frequency: 64 / 7739
Resource:

All diseases associated with this symptom:

AMELOGENESIS IMPERFECTA, TYPE IE (OMIM:301200)
AMELOGENESIS IMPERFECTA, TYPE IF (OMIM:616270)
AMELOGENESIS IMPERFECTA, TYPE IH (OMIM:616221)
Albright hereditary osteodystrophy (Orphanet:665)
Amelo-cerebro-hypohidrotic syndrome (Orphanet:1946)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CLEIDOCRANIAL DYSPLASIA (OMIM:119600)
CODAS syndrome (Orphanet:1458)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cleidocranial dysplasia (Orphanet:1452)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET (OMIM:129540)
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME (OMIM:616029)
ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS (OMIM:600907)
Ectodermal dysplasia - cutaneous syndactyly syndrome (Orphanet:247827)
Ectodermal dysplasia - syndactyly syndrome (Orphanet:247820)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome (Orphanet:313846)
Focal dermal hypoplasia (Orphanet:2092)
Hall-Riggs syndrome (Orphanet:2107)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypercalcemic tumoral calcinosis (Orphanet:306661)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome (Orphanet:363523)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lichstenstein syndrome (Orphanet:2390)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephalic primordial dwarfism, Toriello type (Orphanet:2643)
NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARINGLOSS, AND ENAMEL HYPOPLASIA (OMIM:603641)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodentodigital dysplasia (Orphanet:2710)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Pfeiffer-Palm-Teller syndrome (Orphanet:2871)
Pili torti (Orphanet:2889)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
Pseudopseudohypoparathyroidism (Orphanet:79445)
Rabson-Mendenhall syndrome (Orphanet:769)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SCARF syndrome (Orphanet:3134)
SECKEL SYNDROME 1 (OMIM:210600)
Seckel syndrome (Orphanet:808)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Sjögren-Larsson syndrome (Orphanet:816)
Spondylocarpotarsal synostosis (Orphanet:3275)
Stimmler syndrome (Orphanet:3199)
Timothy syndrome (Orphanet:65283)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A (OMIM:264700)
VITAMIN D-DEPENDENT RICKETS, TYPE 2A (OMIM:277440)
XFE PROGEROID SYNDROME (OMIM:610965)