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2019-10-25
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@cmungall cmungall released this 26 Oct 00:22
· 9626 commits to master since this release
v2019-10-25
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Learn about vigilant mode.
  • remove HP_0000010 'Recurrent urinary tract infections' as a dbxref fr…
  • Fixed id typo , see #890
  • obsoleting generic sucrose intolerance (a phenotype), fixes #886. Axiomatizing other intestinal malabsorbtion diseases
  • revise logical def of 'cystic fibrosis associated meconium ileum'. Addresses #685
  • fix typos. close #873
  • add new term MONDO:0100083 'hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1'. Closes #864
  • revise label, def and synonyms for MONDO_0011071. Closes #863
  • revise labels for hepatitis infection terms. Addresses #825
  • fix ID for 'sleep disorder' in superclass assertion for 'sleep-wake disorder'. Closes #866
  • obsolete MONDO:0005409 variant Creutzfeld Jacob disease. Closes #847
  • add superclass and def for LMNA-related cardiocutaneous progeria syndrome: Addresses #821
  • revise superclasses for 'Hallermann-Streiff syndrome'. addresses #821
  • revise parents and def for De Barsy syndrome. Addresses #821
  • add superclasses and def for acrogeria. Addresses #821
  • revise parent for 'premature aging'. Addresses #821
  • revise text def for 'subcorneal pustular dermatosis'. Addresses #808
  • remove HP: 0001941 as an dbxef to MONDO:0041261 'disorder of acid-base balance'. Addresses #841
  • move MONDO:0001650 'acute cystitis (disease)' to a child of MONDO:0005247 'urinary tract infection (disease)'. Addresses #841
  • remove HP_0000010 'Recurrent urinary tract infections' as a dbxref from MONDO:0001650 'acute cystitis (disease)' and MONDO:0005247 'urinary tract infection (disease)'. Addresses #841
  • add deprecated annotation to synonyms of 'intellectual disability, autosomal recessive 15'. addresses #73
  • delete SubClassOf assertion 'disease has location' some 'hepatobiliary system' (source:EFO:0006513). addresses #834
  • update def for MONDO:0016076. addresses #842

New Classes

Obsoletions

  • MONDO:0005409 variant Creutzfeld Jacob disease --> obsolete variant Creutzfeld Jacob disease
  • MONDO:0045021 sucrose intolerance disease --> obsolete sucrose intolerance disease

Renaming

  • MONDO:0005231 hepatitis C infection --> hepatitis C virus infection
  • MONDO:0005344 hepatitis B infection --> hepatitis B virus infection
  • MONDO:0005354 chronic hepatitis C infection --> chronic hepatitis C virus infection
  • MONDO:0005366 chronic hepatitis B infection --> chronic hepatitis B virus infection
  • MONDO:0005409 variant Creutzfeld Jacob disease --> obsolete variant Creutzfeld Jacob disease
  • MONDO:0005788 hepatitis E infection --> hepatitis E virus infection
  • MONDO:0005789 hepatitis D infection --> hepatitis D virus infection
  • MONDO:0005790 hepatitis A infection --> hepatitis A virus infection
  • MONDO:0008608 down syndrome --> Down syndrome
  • MONDO:0008893 c syndrome --> C syndrome
  • MONDO:0009168 fowler syndrome --> Fowler syndrome
  • MONDO:0009320 hall-Riggs syndrome --> Hall-Riggs syndrome
  • MONDO:0010621 child syndrome --> CHILD syndrome
  • MONDO:0011071 hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome --> hereditary thrombocytopenia and hematologic cancer predisposition syndrome
  • MONDO:0012495 spondyloepimetaphyseal dysplasia, GeneviC(ve type --> spondyloepimetaphyseal dysplasia, Genevieve type
  • MONDO:0018019 Lead poisoning --> lead poisoning
  • MONDO:0045021 sucrose intolerance disease --> obsolete sucrose intolerance disease
Assets 12
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