About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Ectodermal Dysplasia 1, Hypohidrotic, X-Linked; XHED
OMIM ID: 305100
Human Phenotype Ontology associations
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 (3) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     EDA* Eda* View 3 models HGNC
References Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory