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1.

Amelogenesis imperfecta type 1E

Amelogenesis imperfecta is an inherited defect of dental enamel formation that shows both clinical and genetic heterogeneity. In the hypoplastic type of AI, the enamel is of normal hardness but does not develop to normal thickness. The thinness of the enamel makes the teeth appear small. Radiographically, enamel contrasts normally from dentin. The surface of the enamel can vary, showing smooth, rough, pitted, or local forms (Witkop, 1988). [from OMIM]

MedGen UID:
336847
Concept ID:
C1845053
Disease or Syndrome
2.

Amelogenesis imperfecta, type 1J

Amelogenesis imperfecta is an inherited defect of dental enamel formation that shows both clinical and genetic heterogeneity. In the hypoplastic type of AI, the enamel is of normal hardness but does not develop to normal thickness. The thinness of the enamel makes the teeth appear small. Radiographically, enamel contrasts normally from dentin. The surface of the enamel can vary, showing smooth, rough, pitted, or local forms (Witkop, 1988). [from OMIM]

MedGen UID:
934597
Concept ID:
C4310630
Congenital Abnormality
3.

Abnormal dentin morphology

Any abnormality of dentin. [from HPO]

MedGen UID:
866943
Concept ID:
C4021299
Anatomical Abnormality
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