The absence of or defect in the perception of colors. [ NCIT:P378 ]
Synonyms: colour vision deficiency blindness color colour blindness colour vision defects color-vision disease blindness colour color blindness color vision deficiency color vision defects
Term information
- NCIT:C3891 (MONDO:equivalentTo)
- SCTID:193683001 (MONDO:equivalentTo)
- ICD9:368.59 (MONDO:relatedTo)
- Orphanet:98658 (MONDO:equivalentTo)
- DOID:13399 (MONDO:equivalentTo)
- ICD9:368.5 (DOID:13399)
- UMLS:C5681659 (MONDO:equivalentTo)
- MEDGEN:1826147 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, mondo_top_grouping_disorder_of_visual_system, matrix_excluded, otar, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, harrisons_view_disorder_of_visual_system, harrisons_view_psychiatric_disorder, matrix_llm__tag_existing_treatment_other, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, matrix_txgnn_grouping_psychiatric_disorder, ordo_group_of_disorders, harrisons_view_nervous_system_disorder
http://purl.obolibrary.org/obo/NCIT_C3891
http://linkedlifedata.com/resource/umls/id/C5681659
http://www.orpha.net/ORDO/Orphanet_98658
http://identifiers.org/snomedct/193683001
http://identifiers.org/medgen/1826147
http://purl.obolibrary.org/obo/DOID_13399