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: dental enamel hypoplasia

dental enamel hypoplasia Show first 5 Terms
has subtype: amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A ... Show All 18 Terms

amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 1J amelogenesis imperfecta type 1K amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 2A6 amelogenesis imperfecta type 3 amelogenesis imperfecta type 4 X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models