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Grayson-Wilbrandt corneal dystrophy

Go to external page http://purl.obolibrary.org/obo/MONDO_0017391

Grayson-Wilbrandt corneal dystrophy (GWCD) is an extremely rare form of corneal dystrophy characterized by variable patterns of opacification in the Bowman layer of the cornea which extend anteriorly into the epithelium with decreased to normal visual acuity. [ Orphanet:293375 ]

Synonyms: GWCD

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:931248 (MONDO:equivalentTo)
  • GARD:21167 (MONDO:GARD)
  • UMLS:C4305579 (MONDO:equivalentTo)
  • SCTID:717286002 (MONDO:equivalentTo)
  • Orphanet:293375 (MONDO:equivalentTo)
  • icd11.foundation:1667542240 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, ordo_disorder, mondo_top_grouping_disorder_of_visual_system, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, harrisons_view_disorder_of_visual_system, matrix_llm__tag_existing_treatment_other, matrix_included, nord_rare, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, orphanet_rare, mondo_top_grouping_disorder_of_orbital_region

abbreviation
GWCD [ Orphanet:293375 ]

exactMatch

http://identifiers.org/snomedct/717286002

http://linkedlifedata.com/resource/umls/id/C4305579

http://identifiers.org/medgen/931248

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1667542240

http://www.orpha.net/ORDO/Orphanet_293375

id

MONDO:0017391