Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes. [ Orphanet:2908 ]
Term information
- DOID:0060472 (MONDO:equivalentTo)
- Orphanet:2908 (MONDO:equivalentTo)
- GARD:0004391 (Orphanet-shared)
- SCTID:238836000 (MONDO:equivalentTo)
- OMIM:173650 (MONDO:equivalentTo)
- MESH:C536321 (Orphanet:2908)
- ICD10:Q81.8 (Orphanet:2908)
ordo_clinical_subtype
Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes.
http://identifiers.org/snomedct/238836000
http://linkedlifedata.com/resource/umls/id/C0406557
http://identifiers.org/omim/173650
http://www.orpha.net/ORDO/Orphanet_2908
http://purl.obolibrary.org/obo/DOID_0060472
http://identifiers.org/mesh/C536321
hereditary acrokeratotic poikiloderma of Kindler-Weary
poikiloderma of Kindler
Kindler syndrome
KS
KINDLER syndrome
congenital bullous poikiloderma
bullous acrokeratotic poikiloderma of Kindler and Weary
KNDLRS
poikiloderma, congenital, with bullae, Weary type
poikiloderma, hereditary acrokeratotic