About   Help   FAQ
Disease Ontology Browser
Kindler syndrome (DOID:0060472)
Alliance: disease page
Synonyms: hereditary acrokeratotic poikiloderma of Kindler-Weary; poikiloderma of Kindler
Alt IDs: OMIM:173650, MESH:C536321, ORDO:306539
Definition: A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.15
The Jackson Laboratory