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Meesmann corneal dystrophy

Go to external page http://purl.obolibrary.org/obo/MONDO_0007379

Meesmann corneal dystrophy (MECD) is a rare form of superficial corneal dystrophy characterized by distinct tiny bubble-like, round-to-oval punctate bilateral opacities in the central corneal epithelium, and to a lesser extent in the peripheral cornea, with little impact on vision. [ Orphanet:98954 ]

Synonyms: juvenile hereditary epithelial dystrophy of Meesmann juvenile hereditary epithelial dystrophy Meesmann corneal dystrophy MECD stocker-Holt dystrophy juvenile epithelial of Meesmann corneal dystrophy

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0339277 (MONDO:equivalentTo)
  • SCTID:1674008 (MONDO:equivalentTo)
  • MESH:D053559 (Orphanet:98954/e)
  • GARD:9688 (MONDO:GARD)
  • DOID:0060451 (MONDO:equivalentTo)
  • ICD9:371.51 (DOID:0060451)
  • OMIMPS:122100 (MONDO:equivalentTo)
  • NCIT:C84795 (MONDO:equivalentTo)
  • MEDGEN:83283 (MONDO:equivalentTo)
  • Orphanet:98954 (OMIM:122100)
Subsets

gard_rare, matrix_llm__is_cancer_other, ordo_disorder, mondo_top_grouping_disorder_of_visual_system, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, 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, harrisons_view_hereditary_disease, orphanet_rare, mondo_top_grouping_disorder_of_orbital_region

abbreviation
MECD [ DOID:0060451 Orphanet:98954 MONDO:Lexical ]

exactMatch

http://identifiers.org/mesh/D053559

http://identifiers.org/snomedct/1674008

http://linkedlifedata.com/resource/umls/id/C0339277

http://www.orpha.net/ORDO/Orphanet_98954

http://identifiers.org/medgen/83283

http://purl.obolibrary.org/obo/DOID_0060451

https://omim.org/phenotypicSeries/PS122100

http://purl.obolibrary.org/obo/NCIT_C84795

has related synonym

corneal dystrophy, juvenile epithelial of Meesmann

corneal dystrophy, Meesmann epithelial

Meesman dystrophy

Meesmann corneal epithelial dystrophy

corneal dystrophy, Meesmann

corneal dystrophy, juvenile epithelial, of Meesmann

id

MONDO:0007379

seeAlso

https://rarediseases.info.nih.gov/diseases/9688/meesmann-corneal-dystrophy

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml