Search Ontology:
Human Disease

amelogenesis imperfecta

Term ID
DOID:2187
Synonyms
Definition
A dental enamel hypoplasia characterized by abnormal enamel formation. (3)
References
  • GARD:5791
  • ICD10CM:K00.5
  • MESH:D000567
  • MIM:PS104500
  • ORDO:88661
  • SNOMEDCT_US_2023_03_01:78494001
  • UMLS_CUI:C0002452
Ontology
Human Disease   ( DOID:2187 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models
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