Kindler syndrome

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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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: fermt1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008260 - Kindler syndrome

MONDO:0008260 - Kindler syndrome

MIM:

MIM:173650 - KINDLER SYNDROME; KNDLRS

MIM:173650 - KINDLER SYNDROME; KNDLRS

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): skin disease (is_a)