This is just here as a test because I lose it
Term information
database
cross reference
- NANDO:1201004 (https://orcid.org/0000-0003-0011-764X)
- GARD:19952 (MONDO:GARD)
- ICD10CM:Q31.1 (Orphanet:141121/e)
- NANDO:2200190 (https://orcid.org/0000-0003-0011-764X)
- MEDGEN:97973 (MONDO:equivalentTo)
- Orphanet:141121 (MONDO:equivalentTo)
- SCTID:204552001 (MONDO:equivalentTo)
- UMLS:C0396051 (MONDO:equivalentTo)
- icd11.foundation:76585642 (Orphanet:141121)
- ICD9:748.3 (MONDO:relatedTo)
Subsets
gard_rare, ordo_disorder, rare, ordo_malformation_syndrome, nord_rare, orphanet_rare
exactMatch
http://identifiers.org/snomedct/204552001
http://purl.bioontology.org/ontology/ICD10CM/Q31.1
http://identifiers.org/medgen/97973
http://www.orpha.net/ORDO/Orphanet_141121
http://linkedlifedata.com/resource/umls/id/C0396051
Term relations
Subclass of:
- laryngeal disorder
- has characteristic some congenital
- disease has location some subglottis
- disease has major feature some Subglottic stenosis