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Human Disease and Mouse Model Detail
Human Disease Ectodermal Dysplasia 1, Hypohidrotic, X-Linked; XHED
OMIM ID: 305100
Synonyms Christ-Siemens-Touraine Syndrome; CST Syndrome; Ectodermal Dysplasia; Ectodermal Dysplasia 1, Hypohidrotic/Hair/Tooth Type, X-Linked; ECTD1; Ectodermal Dysplasia 1; ED1; Ectodermal Dysplasia, Anhidrotic, X-Linked; EDA; Ectodermal Dysplasia, Hypohidrotic, 1; HED1; EDA1; Xlhed
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Eda* View 2 models 1:0 Homology
     EDA*  
References Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/23/2014
MGI 5.19
The Jackson Laboratory