A rare transmittable degenerative disorder of the brain caused by prions. Morphologically it is characterized by spongiform degeneration of the cerebral and cerebellar cortex. Signs and symptoms include sleep disturbances, personality changes, aphasia, ataxia, muscle atrophy and weakness, visual loss, and myoclonus. It usually leads to death within a year from the onset of the disease. [ NCIT:P378 ]
Synonyms: Jakob-Creutzfeldt disease transmissible virus dementia CJD (Creutzfeldt Jakob disease) Creutzfeldt-Jacob disease Creutzfeldt Jakob Disease Subacute spongiform encephalopathy classic Creutzfeldt-Jakob disease CJD Creutzfeldt Jakob disease Creutzfeldt Jacob syndrome
Term information
- NORD:1014 (MONDO:NORD)
- DOID:11949 (MONDO:equivalentTo)
- MEDGEN:7179 (MONDO:equivalentTo)
- ICD9:046.19 (MONDO:relatedTo)
- EFO:0004226 (MONDO:equivalentTo)
- NCIT:C26802 (MONDO:equivalentTo)
- SCTID:792004 (MONDO:equivalentTo)
- ICD9:046.1 (MONDO:i2s)
- UMLS:C0022336 (MONDO:equivalentTo)
- MESH:D007562 (MONDO:equivalentTo)
gard_rare, harrisons_view_infectious_disease, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, nord_rare, mondo_top_grouping_infectious_disease, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_infectious_disease, matrix_txgnn_grouping_member, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_nervous_system_disorder
http://identifiers.org/snomedct/792004
http://purl.obolibrary.org/obo/DOID_11949
http://www.ebi.ac.uk/efo/EFO_0004226
http://identifiers.org/medgen/7179
http://purl.obolibrary.org/obo/NCIT_C26802
http://identifiers.org/mesh/D007562
http://linkedlifedata.com/resource/umls/id/C0022336