Details of Disease

General Information of Disease (ID: DISPY9IT)

Disease Name Ectodermal dysplasia 13, hair/tooth type
Synonyms ECTD13; ectodermal dysplasia 13, hair/tooth type
Disease Hierarchy
DISLRS4M: Ectodermal dysplasia
DISPY9IT: Ectodermal dysplasia 13, hair/tooth type
Disease Identifiers
MONDO ID
MONDO_0044305
UMLS CUI
C4479322
OMIM ID
617392
MedGen ID
1387448

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
KREMEN1 OTGJFSAC Strong Autosomal recessive [1]
------------------------------------------------------------------------------------

References

1 The Wnt signaling antagonist Kremen1 is required for development of thymic architecture. Clin Dev Immunol. 2006 Jun-Dec;13(2-4):299-319. doi: 10.1080/17402520600935097.