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Echinobase
Summary Literature (0)
DOID:0060472 - Kindler syndrome

Disease Ontology Definition:A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling.

Synonyms: hereditary acrokeratotic poikiloderma of Kindler-Weary, poikiloderma of Kindler,

Echinobase Genes :


OMIM:
MIM:173650 - kindler syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): skin disease (is_a)