Skip to content

v2020-03-05
Compare
Choose a tag to compare
@cmungall cmungall released this 06 Mar 19:57
· 9136 commits to master since this release
v2020-03-05
269db68

Summary:

  • 9 new classes
  • 7 classes obsoleted
  • 27 classes were renamed

Detailed changes:

New Classes

Obsoletions

  • MONDO:0000024 exostoses, multiple --> obsolete exostoses, multiple
  • MONDO:0006697 Chlamydophila infectious disease --> obsolete Chlamydophila infectious disease
  • MONDO:0007065 adenosine deaminase, elevated, hemolytic anemia due to --> obsolete adenosine deaminase, elevated, hemolytic anemia due to
  • MONDO:0008033 autosomal dominant limb-girdle muscular dystrophy type 1B --> obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
  • MONDO:0011809 Mammographic density --> obsolete mammographic density
  • MONDO:0012372 hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features --> obsolete hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features
  • MONDO:0060722 neurodevelopmental disorder with brain, liver, and lung abnormalities --> obsolete neurodevelopmental disorder with brain, liver, and lung abnormalities

Renaming

  • MONDO:0000024 exostoses, multiple --> obsolete exostoses, multiple
  • MONDO:0005775 glucosephosphate dehydrogenase deficiency --> G6PD deficiency
  • MONDO:0006697 Chlamydophila infectious disease --> obsolete Chlamydophila infectious disease
  • MONDO:0007065 adenosine deaminase, elevated, hemolytic anemia due to --> obsolete adenosine deaminase, elevated, hemolytic anemia due to
  • MONDO:0008033 autosomal dominant limb-girdle muscular dystrophy type 1B --> obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
  • MONDO:0010433 SLEB15 --> systemic lupus erythematosus, susceptibility to, 15
  • MONDO:0010624 ichthyosis follicularis-alopecia-photophobia syndrome --> IFAP/Breshek syndrome
  • MONDO:0010898 familial temporal lobe epilepsy 1 --> Autosomal dominant epilepsy with auditory features
  • MONDO:0011560 SLEB3 --> systemic lupus erythematosus, susceptibility to, 3
  • MONDO:0011807 SLEH1 --> systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1
  • MONDO:0011809 Mammographic density --> obsolete mammographic density
  • MONDO:0011942 SLEN1 --> systemic lupus erythematosus with nephritis, susceptibility to, 1
  • MONDO:0011943 SLEN2 --> systemic lupus erythematosus with nephritis, susceptibility to, 2
  • MONDO:0011944 SLEN3 --> systemic lupus erythematosus with nephritis, susceptibility to, 3
  • MONDO:0012036 SLEB4 --> systemic lupus erythematosus, susceptibility to, 4
  • MONDO:0012361 SLEB5 --> systemic lupus erythematosus, susceptibility to, 5
  • MONDO:0012369 SLEB6 --> systemic lupus erythematosus, susceptibility to, 6
  • MONDO:0012372 hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features --> obsolete hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features
  • MONDO:0012403 SLEB7 --> systemic lupus erythematosus, susceptibility to, 7
  • MONDO:0012404 SLEB8 --> systemic lupus erythematosus, susceptibility to, 8
  • MONDO:0012836 SLEB12 --> systemic lupus erythematosus, susceptibility to, 12
  • MONDO:0012884 SLEB13 --> systemic lupus erythematosus, susceptibility to, 13
  • MONDO:0013152 SLEB14 --> systemic lupus erythematosus, susceptibility to, 14
  • MONDO:0013731 early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome --> MEGF10-Related Myopathy
  • MONDO:0013743 autosomal systemic lupus erythematosus --> autosomal systemic lupus erythematosus type 16
  • MONDO:0020135 non-syndromic pontocerebellar hypoplasia --> pontocerebellar hypoplasia
  • MONDO:0060722 neurodevelopmental disorder with brain, liver, and lung abnormalities --> obsolete neurodevelopmental disorder with brain, liver, and lung abnormalities

Also available here changes.md

Assets 12
Loading