v2020-06-01

New Classes

• MONDO:0020789 pseudo-TORCH syndrome 1
• MONDO:0020790 gaze palsy, familial horizontal, with progressive scoliosis 1
• MONDO:0020791 corneal dystrophy, meesmann, 1
• MONDO:0020792 dwarfism with tall vertebrae
• MONDO:0100125 hallucinogen-persisting perception disorder
• MONDO:0100130 adult acute respiratory distress syndrome
• MONDO:0100131 pediatric acute respiratory distress syndrome

Obsoletions

• MONDO:0001012 breast fibroadenosis --> obsolete breast fibroadenosis
• MONDO:0010249 X-linked B cell surface antigen, mouse, homolog-like 1 --> obsolete X-linked B cell surface antigen, mouse, homolog-like 1
• MONDO:0013596 nonsyndromic congenital nail disorder 10 --> obsolete nonsyndromic congenital nail disorder 10
• MONDO:0015963 inherited renal tumor --> obsolete inherited renal tumor
• MONDO:0015966 hereditary eye tumor --> obsolete hereditary eye tumor
• MONDO:0015981 inherited gynecological tumor --> obsolete inherited gynecological tumor
• MONDO:0021062 hereditary acrokeratotic poikiloderma of Kindler-Weary --> obsolete hereditary acrokeratotic poikiloderma of Kindler-Weary
• MONDO:0023310 hemiplegic migraine --> obsolete hemiplegic migraine
• MONDO:0023873 noonan-like/multiple giant cell lesion syndrome --> obsolete Noonan-like/multiple giant cell lesion syndrome
• MONDO:0024597 CD3epsilon deficiency --> obsolete CD3epsilon deficiency

Renaming

• MONDO:0001012 breast fibroadenosis --> obsolete breast fibroadenosis
• MONDO:0001627 dementia --> dementia (disease)
• MONDO:0006502 adult respiratory distress syndrome --> acute respiratory distress syndrome
• MONDO:0008319 protoporphyria, erythropoietic --> protoporphyria, erythropoietic, 1
• MONDO:0010249 X-linked B cell surface antigen, mouse, homolog-like 1 --> obsolete X-linked B cell surface antigen, mouse, homolog-like 1
• MONDO:0013596 nonsyndromic congenital nail disorder 10 --> obsolete nonsyndromic congenital nail disorder 10
• MONDO:0014006 intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome --> Schuurs-Hoeijmakers syndrome
• MONDO:0015023 nemaline myopathy 11 --> MYPN-related myopathy
• MONDO:0015653 monogenic disease with epilepsy --> monogenic epilepsy
• MONDO:0015951 genetic photodermatosis --> hereditary photodermatosis
• MONDO:0015963 inherited renal tumor --> obsolete inherited renal tumor
• MONDO:0015966 hereditary eye tumor --> obsolete hereditary eye tumor
• MONDO:0015981 inherited gynecological tumor --> obsolete inherited gynecological tumor
• MONDO:0021062 hereditary acrokeratotic poikiloderma of Kindler-Weary --> obsolete hereditary acrokeratotic poikiloderma of Kindler-Weary
• MONDO:0023310 hemiplegic migraine --> obsolete hemiplegic migraine
• MONDO:0023873 noonan-like/multiple giant cell lesion syndrome --> obsolete Noonan-like/multiple giant cell lesion syndrome
• MONDO:0024597 CD3epsilon deficiency --> obsolete CD3epsilon deficiency
• MONDO:0025481 zoonoses --> zoonosis
• MONDO:0026733 intellectual developmental disorder, x-linked, syndromic, hackmann-di donato type --> intellectual developmental disorder, x-linked, syndromic, Hackmann-Di Donato type
• MONDO:0032668 diamond-blackfan anemia 18 --> Diamond-Blackfan anemia 18
• MONDO:0032669 diamond-blackfan anemia 19 --> Diamond-Blackfan anemia 19
• MONDO:0032670 diamond-blackfan anemia 20 --> Diamond-Blackfan anemia 20
• MONDO:0032791 coffin-siris syndrome 10 --> Coffin-Siris syndrome 10
• MONDO:0032793 o'donnell-luria-rodan syndrome --> O'Donnell-Luria-Rodan syndrome
• MONDO:0032841 usher syndrome, type 1m --> Usher syndrome, type 1M
• MONDO:0032882 heyn-sproul-jackson syndrome --> Heyn-Sproul-Jackson syndrome
• MONDO:0032885 spondyloepimetaphyseal dysplasia, isidor-toutain type --> spondyloepimetaphyseal dysplasia, Isidor-Toutain type
• MONDO:0032886 liang-wang syndrome --> Liang-Wang syndrome
• MONDO:0032889 poirier-bienvenu neurodevelopmental syndrome --> Poirier-Bienvenu neurodevelopmental syndrome
• MONDO:0032901 catifa syndrome --> Catifa syndrome
• MONDO:0032902 joubert syndrome 36 --> Joubert syndrome 36
• MONDO:0032904 corneal dystrophy, meesmann, 2 --> corneal dystrophy, Meesmann, 2
• MONDO:0032908 cebalid syndrome --> CEBALID syndrome
• MONDO:0032912 coffin-siris syndrome 11 --> Coffin-Siris syndrome 11
• MONDO:0032915 long qt syndrome 16 --> long QT syndrome 16
• MONDO:0032916 imagawa-matsumoto syndrome --> Imagawa-Matsumoto syndrome
• MONDO:0032922 beck-fahrner syndrome --> Beck-Fahrner syndrome
• MONDO:0044309 diamond-blackfan anemia 16 --> Diamond-Blackfan anemia 16
• MONDO:0044310 diamond-blackfan anemia 17 --> Diamond-Blackfan anemia 17
• MONDO:0054588 noonan syndrome-like disorder with loose anagen hair 2 --> Noonan syndrome-like disorder with loose anagen hair 2
• MONDO:0100101 Fetal akinesia deformation sequence 1 --> fetal akinesia deformation sequence 1
• MONDO:0100102 Fetal akinesia deformation sequence 2 --> fetal akinesia deformation sequence 2
• MONDO:0100103 Fetal akinesia deformation sequence 3 --> fetal akinesia deformation sequence 3
• MONDO:0100104 Fetal akinesia deformation sequence 4 --> fetal akinesia deformation sequence 4