v2021-04-30
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6301 commits
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since this release
New Classes
- MONDO:0030962 nephrotic syndrome, type 23
- MONDO:0030965 olmsted syndrome 2
- MONDO:0030971 immunodeficiency 78 with autoimmunity and developmental delay
- MONDO:0030973 immunodeficiency 77
- MONDO:0030974 mitochondrial complex 2 deficiency, nuclear type 4
- MONDO:0030981 immunodeficiency 79
- MONDO:0030985 premature ovarian failure 19
- MONDO:0030989 spermatogenic failure 53
- MONDO:0030996 bleeding disorder, platelet-type, 24
- MONDO:0030997 mitochondrial complex 1 deficiency, nuclear type 37
- MONDO:0030998 deafness, autosomal dominant 80
- MONDO:0031003 hypercholanemia, familial, 2
- MONDO:0031009 Glanzmann thrombasthenia 2
- MONDO:0031010 odontochondrodysplasia 2 with hearing loss and diabetes
- MONDO:0031037 famililal cerebral cavernous malformations
- MONDO:0031169 odontochondrodysplasia
- MONDO:0031332 Glanzmann thrombasthenia 1
- MONDO:0031446 hypercholanemia, familial 1
- MONDO:0031481 microcephaly, epilepsy, and diabetes syndrome 1
- MONDO:0100308 atactic disorder
- MONDO:0100309 hereditary ataxia
- MONDO:0100310 hereditary cerebellar ataxia
- MONDO:0100311 sensory ataxia
- MONDO:0100312 vestibular ataxia
- MONDO:0100318 COVID-19 or sequela
- MONDO:0100319 COVID-19–associated multisystem inflammatory syndrome in adults
- MONDO:0100320 sequela of COVID-19
- MONDO:0100321 viral disease or post-viral disorder
- MONDO:0100325 odontochondrodysplasia 1
- MONDO:0100326 Glanzmann thrombasthenia
- MONDO:0100327 hypercholanemia, familial
- MONDO:0100328 microcephaly, epilepsy, and diabetes syndrome
- MONDO:0100337 SEC61A1 deficiency
- MONDO:0100339 Friedreich ataxia
- MONDO:0100340 Friedreich ataxia 1
- MONDO:0100342 malignant glioma
- MONDO:0100343 antenatal Bartter syndrome
- MONDO:0100344 Bartter disease type 1
- MONDO:0100345 lactose intolerance (disease)
- MONDO:0100347 carcinoid syndrome
Obsoletions
- MONDO:0000557 hereditary ataxia --> obsolete hereditary ataxia
- MONDO:0006689 carcinoid syndrome --> obsolete carcinoid syndrome
- MONDO:0007291 familial cerebral cavernous malformation --> obsolete familial cerebral cavernous malformation
- MONDO:0008480 odontochondrodysplasia --> obsolete odontochondrodysplasia
- MONDO:0009116 lactose intolerance (disease) --> obsolete lactose intolerance (disease)
- MONDO:0009245 Friedreich ataxia --> obsolete Friedreich ataxia
- MONDO:0010119 Glanzmann's thrombasthenia --> obsolete Glanzmann's thrombasthenia
- MONDO:0011127 Bartter disease type 1 --> obsolete Bartter disease type 1
- MONDO:0011905 familial hypercholanemia --> obsolete familial hypercholanemia
- MONDO:0013647 primary microcephaly-epilepsy-permanent neonatal diabetes syndrome --> obsolete primary microcephaly-epilepsy-permanent neonatal diabetes syndrome
- MONDO:0015917 malignant glioma --> obsolete malignant glioma
- MONDO:0100139 asymptomatic COVID-19 infection --> obsolete asymptomatic COVID-19 infection
- MONDO:0100140 mild COVID-19 infection --> obsolete mild COVID-19 infection
- MONDO:0100141 moderate COVID-19 infection --> obsolete moderate COVID-19 infection
- MONDO:0100142 severe COVID-19 infection --> obsolete severe COVID-19 infection
- MONDO:0100143 critical COVID-19 infection --> obsolete critical COVID-19 infection
- MONDO:0100145 presymptomatic COVID-19 infection --> obsolete presymptomatic COVID-19 infection
Renaming
- MONDO:0000557 hereditary ataxia --> obsolete hereditary ataxia
- MONDO:0005227 abscess --> abscess (disease)
- MONDO:0006689 carcinoid syndrome --> obsolete carcinoid syndrome
- MONDO:0007291 familial cerebral cavernous malformation --> obsolete familial cerebral cavernous malformation
- MONDO:0008480 odontochondrodysplasia --> obsolete odontochondrodysplasia
- MONDO:0009116 lactose intolerance (disease) --> obsolete lactose intolerance (disease)
- MONDO:0009245 Friedreich ataxia --> obsolete Friedreich ataxia
- MONDO:0010119 Glanzmann's thrombasthenia --> obsolete Glanzmann's thrombasthenia
- MONDO:0011127 Bartter disease type 1 --> obsolete Bartter disease type 1
- MONDO:0011905 familial hypercholanemia --> obsolete familial hypercholanemia
- MONDO:0013647 primary microcephaly-epilepsy-permanent neonatal diabetes syndrome --> obsolete primary microcephaly-epilepsy-permanent neonatal diabetes syndrome
- MONDO:0014195 microcornea-myopic chorioretinal atrophy-telecanthus syndrome --> microcornea-myopic chorioretinal atrophy
- MONDO:0015917 malignant glioma --> obsolete malignant glioma
- MONDO:0020724 familial cerebral cavernous malformation 1 --> cerebral cavernous malformation 1
- MONDO:0026767 immunodeficiency 74, covid19-related, X-linked --> immunodeficiency 74, COVID-19-related, X-linked
- MONDO:0100139 asymptomatic COVID-19 infection --> obsolete asymptomatic COVID-19 infection
- MONDO:0100140 mild COVID-19 infection --> obsolete mild COVID-19 infection
- MONDO:0100141 moderate COVID-19 infection --> obsolete moderate COVID-19 infection
- MONDO:0100142 severe COVID-19 infection --> obsolete severe COVID-19 infection
- MONDO:0100143 critical COVID-19 infection --> obsolete critical COVID-19 infection
- MONDO:0100145 presymptomatic COVID-19 infection --> obsolete presymptomatic COVID-19 infection