Details of Disease

General Information of Disease (ID: DISWS0HI)

Disease Name Amelogenesis imperfecta, hypomaturation type, IIa6
Synonyms AI2A6; amelogenesis imperfecta, hypomaturation type, IIa6; amelogenesis imperfecta, hypomaturation type, IIa6; AI2A6
Disease Hierarchy
DISX8NN4: Amelogenesis imperfecta type 2
DISWS0HI: Amelogenesis imperfecta, hypomaturation type, IIa6
Disease Identifiers
MONDO ID
MONDO_0014971
UMLS CUI
C4310665
OMIM ID
617217
MedGen ID
934632

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
GPR68 OT1NXSMN Strong Autosomal recessive [1]
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References

1 Proton-sensing G-protein-coupled receptors. Nature. 2003 Sep 4;425(6953):93-8. doi: 10.1038/nature01905.