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congenital laryngeal web

Go to external page http://purl.obolibrary.org/obo/MONDO_0007880

Congenital laryngeal web is a rare malformation consisting of a membrane-like structure that extends across the laryngeal lumen close to the level of the vocal cords. [ Orphanet:2374 ]

Synonyms: Laryngeal web

This is just here as a test because I lose it

Term information

database cross reference
  • SCTID:444921008 (MONDO:equivalentTo)
  • Orphanet:2374 (OMIM:150360)
  • OMIM:150360 (Orphanet:2374/e)
  • MESH:C563636 (MONDO:equivalentTo)
  • UMLS:C1835494 (MONDO:equivalentTo)
  • NCIT:C98970 (MONDO:equivalentTo)
  • MESH:C537676 (MONDO:equivalentTo)
  • MEDGEN:372058 (MONDO:equivalentTo)
  • GARD:16596 (MONDO:GARD)
  • MedDRA:10023871 (Orphanet:2374/e)
Subsets

ordo_disorder, gard_rare, otar, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4069

closeMatch

http://identifiers.org/meddra/10023871

exactMatch

http://identifiers.org/medgen/372058

http://purl.obolibrary.org/obo/NCIT_C98970

http://identifiers.org/mesh/C563636

http://identifiers.org/snomedct/444921008

https://omim.org/entry/150360

http://identifiers.org/mesh/C537676

http://www.orpha.net/ORDO/Orphanet_2374

http://linkedlifedata.com/resource/umls/id/C1835494

has related synonym

laryngeal web, congenital heart disease and low stature

subglottic web

laryngeal web, familial

subglottic bar, congenital heart disease and low stature

gay Feinmesser Cohen syndrome

glottic web, congenital anterior

subglottic Bar

id

MONDO:0007880

seeAlso

https://rarediseases.info.nih.gov/diseases/2446/gay-feinmesser-cohen-syndrome

Term relations