ZFIN Human Disease: peeling skin syndrome

OBO ID: DOID:0060283

Term Name:	peeling skin syndrome		Search Ontology:
Synonyms:	deciduous skin familial continuous skin peeling syndrome keratosis exfoliativa congenita peeling skin disease
Definition:	A skin disease that is characterized by the painless, continuous peeling of the top layer of skin. https://rarediseases.org/rare-diseases/peeling-skin-syndrome/
References:	GARD:7347 MESH:C564818 OMIM:PS270300 ORDO:817 SNOMEDCT_US_2023_03_01:724838009 UMLS_CUI:C1849193
Ontology:	Human Disease ( DOID:0060283 )

Relationships

is a type of:	autosomal recessive disease skin disease autosomal recessive disease skin disease Show first 5 Terms
has subtype:	peeling skin syndrome 1 peeling skin syndrome 2 peeling skin syndrome 3 peeling skin syndrome 4 peeling skin syndrome 5 ... Show All 6 Terms peeling skin syndrome 1 peeling skin syndrome 2 peeling skin syndrome 3 peeling skin syndrome 4 peeling skin syndrome 5 peeling skin syndrome 6 Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None