Partial or complete opacity of the crystalline lens of one or both eyes that decreases visual acuity and eventually results in blindness. Some cataracts appear in infancy or in childhood, but most develop in older individuals. (Sternberg Diagnostic Surgical Pathology, 3rd ed.) [ NCIT:C26713 ]

Synonyms: opacity of the lens cataract cataract (disease)

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:366.9 (MONDO:i2s)
  • MEDGEN:39462 (MONDO:equivalentTo)
  • UMLS:C0086543 (MONDO:equivalentTo)
  • DOID:83 (MONDO:equivalentTo)
  • icd11.foundation:109841337 (MONDO:equivalentTo)
  • NCIT:C26713 (NCIT:C26713)
  • ICD9:366.8 (MONDO:relatedTo)
  • OMIMPS:116200 (https://orcid.org/0000-0002-6601-2165)
  • ICD9:366 (EFO:0001059)
  • SCTID:193570009 (MONDO:equivalentTo)
  • MESH:D002386 (MONDO:equivalentTo)
  • ICD9:366.44 (MONDO:relatedTo)
  • HP:0000518 (MONDO:otherHierarchy)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, mondo_top_grouping_disorder_of_visual_system, matrix_excluded, 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_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_orbital_region

OBO foundry unique label

cataract (disease)

exactMatch

http://identifiers.org/medgen/39462

http://linkedlifedata.com/resource/umls/id/C0086543

http://purl.obolibrary.org/obo/DOID_83

http://identifiers.org/mesh/D002386

http://purl.obolibrary.org/obo/NCIT_C26713

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/109841337

https://omim.org/phenotypicSeries/PS116200

http://identifiers.org/snomedct/193570009

id

MONDO:0005129

should conform to

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