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Releases: DiseaseOntology/HumanDiseaseOntology

DO's mid October 2023 release

21 Oct 17:40
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This DO release includes 11,386 diseases, 8,276 SubClassOf and 726 EQ axioms. This release includes the addition of 13 disease terms, 19 definitions, 25 SubClassOf axioms and 1 EQ axiom. New and revised content includes: added synonyms for autosomal recessive spinocerebellar ataxia; the addition of autosomal recessive spinocerebellar ataxia, amyotrophic lateral sclerosis subtypes; revised classifications for schwannomatosis and neurofibromatosis, rhabdomyosarcoma,;the addition of new disease terms: Legius syndrome and Watson syndrome, diphthamide deficiency syndrome and subtypes, renal medullary carcinoma; augmentation of the DO_cancer_slim, updated nomenclature for thyroid cancer and a revised NCIthesaurus slim, produced programmatically based on NCI xrefs or skis mappings.

DO September 2023 release

29 Sep 04:04
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This release of the Human Disease Ontology includes 11,373 disease classes, 9,003 with textual definitions (79.2%). Updates include revised mappings based on UMLS 2023AA; the addition of early-onset epilepsy 2 & 3, Yoon-Bellen neurodevelopmental syndrome, NEDDFAC, SCAN3 and updates to other SCAN diseases; revision of viral infectious diseases to incorporate official viral nomenclature changes from ICTV; reactivation of Epstein-Barr virus infectious disease; and various definition updates & corrections.

DO early August release

08 Aug 12:43
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This release includes a major fix to recently added diseases. Five diseases were added in the June 2023 release with duplicate IRIs matching historically obsoleted diseases (pre-2015). These diseases with duplicate IRIs have been deleted and re-added with new, unique IRIs as follows:

  • disabling pansclerotic morphea, DOID:0080002 -> DOID:0081373
  • nemaline myopathy 5B, DOID:0080003 -> DOID:0081374
  • nemaline myopathy 5C, DOID:0080004 -> DOID:0081375
  • sorbitol dehydrogenase deficiency with peripheral neuropathy, DOID:0080025 -> DOID:0081376
  • COX deficiency, benign infantile mitochondrial myopathy, DOID:0080035 -> DOID:0081377

If at all possible, use THIS release instead of the June and July releases (v2023-06-29, v2023-07-20 & v2023-07-24).

We apologize for any inconvenience this may have caused.

DO July 2023 release -- minor revision

24 Jul 19:50
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Minor fix to inheritance information in two textual definitions.

If at all possible, DO NOT USE this release; instead, use the early August release v2023-08-08 or later. This release includes accidental IRI duplicates that are not consistent or compatible with previous or future releases. These duplicate disease IRIs were deleted and the diseases re-added with new, unique IRIs in release v2023-08-08.

Human Disease Ontology July 2023 release

21 Jul 14:53
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This release of the Human Disease Ontology includes 11,367 disease classes, 8,996 with textual definitions (79.1%). Updates include revision and addition to disease classifications for carpal tunnel syndromes, mitochondrial complex V deficiency diseases, hereditary spastic paraplegias, xanthinuria diseases, and cone-rod dystrophies, along with corrections to spelling and ICD10CM cross-references.

Full Changelog: v2023-06-29...v2023-07-20

If at all possible, DO NOT USE this release; instead, use the early August release v2023-08-08 or later. This release includes accidental IRI duplicates that are not consistent or compatible with previous or future releases. These duplicate disease IRIs were deleted and the diseases re-added with new, unique IRIs in release v2023-08-08.

DO's June 2023 release

29 Jun 15:43
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DO's June 2023 release. Includes 11,349 disease terms, the addition of 35 new diseases, 42 new SubClassOf axioms. This release includes reformatting of gene symbols in definitions, the addition of mtDNA depletion syndrome subtypes 16-20, retinal macular dystrophy and subtypes, sorbitol dehydrogenase deficiency with peripheral neuropathy, hyperphosphatasia with impaired intellectual development syndrome subtypes, revised nemaline classification and COX deficiency classification, new digenic disease annotations.

If at all possible, DO NOT USE this release; instead, use the early August release v2023-08-08 or later. This release includes accidental IRI duplicates that are not consistent or compatible with previous or future releases. These duplicate disease IRIs were deleted and the diseases re-added with new, unique IRIs in release v2023-08-08.

DO's May 2023 release

31 May 15:55
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This release includes 11,314 disease terms and 8,942 textual definitions (79.0%) with added definitions, xrefs, new DO terms and revised classifications. Included are updates for bradyopsia, NBCCS - nevoid basal cell carcinoma syndrome, leukoencephalopathy with vanishing white matter, developmental and epileptic encephalopathy, hypomyelinating leukodystrophy, epidermolytic hyperkeratosis, autosomal recessive spinocerebellar ataxia, Paget's disease of bone, spastic quadriplegic cerebral palsy, spinal muscular atrophy and various myopathies. Added diseases include acrocardiofacial syndrome, Hengel-Maroofian-Schols syndrome, early onset progressive encephalopathy with brain atrophy and thin corpus callosum, Luo-Schoch-Yamamoto syndrome and Pierpont syndrome, along with many others.

DO's March 2023 release

31 Mar 18:06
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This release includes 11,224 disease terms, 8,846 textual definitions, 724 EQ axioms and 8,124 SubClassOf axioms; an increase of 8 new disease terms, 10 new definitions, 2 EQs, 33 SubClassOf axioms. This release included updating of disease names, synonyms and xrefs and associated phenotypes, updates of classifications for frontotemporal dementia, major depressive disorder and related classes and updated COPD definitions, chronic granulomatous, and glycogen storage diseases and hypoglycemia disease annotations and the addition of an axiom to define prion disease, progeria disease subtypes, chronic granulomatous disease 5.

DO's February Release

27 Feb 16:42
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DO February 2023 release: 11,216 disease terms. This release included the addition of new disease terms, definitions and nomenclature updates, and review and updates of rare diseases in the DO, including lymphoma nomenclature updates; the addition of new disease terms: breast implant illness; neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss; myoclonic-atonic epilepsy; oxoglutarate dehydrogenase deficiency; and neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures. And the addition of a new DOreport for DO's cancer branch: new DO-ICDO-anatomy DOreport.

January 2023 release Human Disease Ontology

30 Jan 22:45
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DO's January 2023 release includes 11,207 disease terms, with 8,820 (78.7%) textual definitions. 26 new disease terms, 76 new definitions. This release includes a new DO_infectious_disease_slim; updated xrefs from our bi-annual UMLS update, including all SNOMED_CT xrefs to the latest release; the annotation of trinucleotide repeat expansion disorders, digenic and polygenic disease annotations, a revised VEXAS syndrome, the addition of bronchopulmonary dysplasia and intellectual developmental disorder with ocular anomalies and distinctive facial features, numerous CNS neoplasm terms and their associated ICDO codes.