peeling skin syndrome

Summary

DOID:0060283 - peeling skin syndrome

Disease Ontology Definition:A skin disease that is characterized by the painless, continuous peeling of the top layer of skin.

Synonyms: deciduous skin, familial continuous skin peeling syndrome, keratosis exfoliativa congenita, peeling skin disease, PSS

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

: tgm5, chst8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019347 - peeling skin syndrome

MONDO:0019347 - peeling skin syndrome

MIM:

MIM:270300 - PEELING SKIN SYNDROME 1; PSS1
MIM:613088 - PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO, 2

MIM:270300 - PEELING SKIN SYNDROME 1; PSS1

MIM:613088 - PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO, 2

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

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

Parent(s): autosomal recessive disease (is_a), skin disease (is_a)