Details of Disease

General Information of Disease (ID: DISUYYW8)

Disease Name Amelogenesis imperfecta type 3B
Synonyms amelogenesis imperfecta, type IIIB; AI3B; amelogenesis imperfecta, type 3B
Disease Hierarchy
DISGYR9E: Amelogenesis imperfecta
DISUYYW8: Amelogenesis imperfecta type 3B
Disease Identifiers
MONDO ID
MONDO_0021547
UMLS CUI
C4539891
OMIM ID
617607
MedGen ID
1621302

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
AMTN OTXAMT4V Limited Autosomal dominant [1]
------------------------------------------------------------------------------------

References

1 Enamel Hypomineralization and Structural Defects in Amelotin-deficient Mice. J Dent Res. 2015 May;94(5):697-705. doi: 10.1177/0022034514566214. Epub 2015 Feb 24.