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Amelogenesis imperfecta, type 3A(AI3A)

MedGen UID:: 1054097
•Concept ID:: CN377797
•: Disease or Syndrome

Synonyms:	AI3A; AMELOGENESIS IMPERFECTA, TYPE IIIA; AMELOGENESIS IMPERFECTA, TYPE IIIA, LOCALIZED

Monarch Initiative:	MONDO:0007538
OMIM®:	130900

Definition

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the FAM83H gene. [from MONDO]

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GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVAmelogenesis imperfecta

Abnormality of the musculoskeletal system
- Abnormality of connective tissue
  - Abnormal odontoid tissue morphology
    - Abnormal dental enamel morphology
      - Amelogenesis imperfecta
        Amelogenesis imperfecta, hypocalcification type
        Amelogenesis imperfecta, type 3A

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Amelogenesis imperfecta, type 3A
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