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Kindler syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0008260

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 ]

This is just here as a test because I lose it

Term information

database cross reference
  • 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)
Subsets

ordo_clinical_subtype

Synonym to be removed from public release but maintained in edit version as record of external usage
hereditary acrokeratotic poikiloderma of Kindler-Weary [ DOID:0060472 ]

abbreviation
KS [ Orphanet:2908 ]

definition

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.

exactMatch

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

excluded from QC check

http://purl.obolibrary.org/obo/mondo/sparql/single-child-tags.sparql

has exact synonym

hereditary acrokeratotic poikiloderma of Kindler-Weary

poikiloderma of Kindler

Kindler syndrome

KS

has related synonym

KINDLER syndrome

congenital bullous poikiloderma

bullous acrokeratotic poikiloderma of Kindler and Weary

KNDLRS

poikiloderma, congenital, with bullae, Weary type

poikiloderma, hereditary acrokeratotic

id

MONDO:0008260