Hypoplasia of dental enamel
Symptom Information:
Symptom ID: | HPO:0006297 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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) |