JSON

KID syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0018781

Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss. [ Orphanet:477 ]

Synonyms: KID/HID syndrome Keratitis Ichthyosis Deafness Syndrome keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome Senter syndrome ichthyosis hystrix Rheydt type

This is just here as a test because I lose it

Term information

database cross reference
  • MedDRA:10048786 (Orphanet:477/e)
  • UMLS:C3665333 (MONDO:equivalentTo)
  • MEDGEN:777082 (MONDO:equivalentTo)
  • NANDO:2200996 (https://orcid.org/0000-0003-0011-764X)
  • MESH:C536168 (MONDO:equivalentTo)
  • OMIMPS:148210 (MONDO:equivalentTo)
  • SCTID:2625009 (MONDO:equivalentTo)
  • Orphanet:477 (MONDO:equivalentTo)
  • NORD:1326 (MONDO:NORD)
  • GARD:3113 (MONDO:GARD)
  • NANDO:1200621 (https://orcid.org/0000-0003-0011-764X)
  • ICD9:759.89 (MONDO:relatedTo)
Subsets

gard_rare, ordo_disorder, otar, ordo_inheritance_inconsistent, rare, nord_rare, orphanet_rare

closeMatch

http://identifiers.org/meddra/10048786

comment

Editor note: Orphanet classifies as both AD and AR

exactMatch

http://www.orpha.net/ORDO/Orphanet_477

http://linkedlifedata.com/resource/umls/id/C3665333

https://omim.org/phenotypicSeries/PS148210

http://identifiers.org/mesh/C536168

http://identifiers.org/snomedct/2625009

http://identifiers.org/medgen/777082

has related synonym

keratitis, ichthyosis, and deafness (KID) syndrome

id

MONDO:0018781