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DO September 2024 release
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allenbaron committed Sep 27, 2024
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18 changes: 16 additions & 2 deletions DOreports/DO-subClassOf-anonymous.tsv
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Expand Up @@ -385,6 +385,7 @@ DOID:0050813 spondyloepiphyseal dysplasia with congenital joint dislocations 'di
DOID:0050814 temtamy preaxial brachydactyly syndrome 'has material basis in' some 'autosomal recessive inheritance'
DOID:0050816 urofacial syndrome 'has material basis in' some 'autosomal recessive inheritance'
DOID:0050827 rheumatic heart disease 'has symptom' some inflammation
DOID:0050829 pericardium disease 'disease has location' some 'thoracic segment of trunk'
DOID:0050831 familial encephalopathy with neuroserpin inclusion bodies 'has material basis in' some 'autosomal dominant inheritance'
DOID:0050841 focal hand dystonia 'disease has location' some hand
DOID:0050849 periampullary adenoma ('derives from' some 'epithelial cell') and (has_origin some gland)
Expand Down Expand Up @@ -716,7 +717,7 @@ DOID:0060717 autosomal recessive congenital ichthyosis 8 'disease has basis in'
DOID:0060718 autosomal recessive congenital ichthyosis 9 'disease has basis in' some 'Abnormality of prenatal development or birth'
DOID:0060719 autosomal recessive congenital ichthyosis 10 'disease has basis in' some 'Abnormality of prenatal development or birth'
DOID:0060720 autosomal recessive congenital ichthyosis 11 'disease has basis in' some 'Abnormality of prenatal development or birth'
DOID:0060728 NGLY1-deficiency 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060728 congenital disorder of deglycosylation 1 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060730 torsion dystonia 1 'has material basis in' some 'autosomal dominant inheritance'
DOID:0060731 congenital central hypoventilation syndrome 'disease has basis in' some 'Abnormality of prenatal development or birth'|'has material basis in' some 'autosomal dominant inheritance'
DOID:0060733 junctional epidermolysis bullosa with pyloric atresia 'has material basis in' some 'autosomal recessive inheritance'
Expand Down Expand Up @@ -885,6 +886,16 @@ DOID:0060978 Fanconi anemia complementation group W 'has material basis in' some
DOID:0060979 Fanconi anemia complementation group S 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060981 mosaic variegated aneuploidy syndrome 4 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060983 sitosterolemia 2 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060984 digenic dyskeratosis congenita 'has material basis in' some 'digenic inheritance'
DOID:0060985 preaxial polydactyly type IV 'has material basis in' some 'autosomal dominant inheritance'
DOID:0060986 preaxial polydactyly II 'has material basis in' some 'autosomal dominant inheritance'
DOID:0060987 preaxial polydactyly I 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060988 pancreatic agenesis 2 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060989 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1 'has material basis in' some 'autosomal dominant inheritance'
DOID:0060990 congenital disorder of deglycosylation 2 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060992 bent bone dysplasia syndrome 1 'has material basis in' some 'autosomal dominant inheritance'
DOID:0060993 bent bone dysplasia syndrome 2 'has material basis in' some 'autosomal recessive inheritance'
DOID:0060994 encephalopathy due to defective mitochondrial and peroxisomal fission 2 'has material basis in' some 'autosomal recessive inheritance'
DOID:0070000 3-methylglutaconic aciduria type 8 'has material basis in' some 'autosomal recessive inheritance'
DOID:0070002 3-methylglutaconic aciduria type 9 'has material basis in' some 'autosomal recessive inheritance'
DOID:0070014 autosomal dominant dyskeratosis congenita 1 'has material basis in' some 'autosomal dominant inheritance'
Expand Down Expand Up @@ -1263,6 +1274,7 @@ DOID:0070596 X-linked spermatogenic failure 5 'has material basis in' some 'X-li
DOID:0070597 X-linked spermatogenic failure 6 'has material basis in' some 'X-linked inheritance'
DOID:0070598 X-linked spermatogenic failure 7 'has material basis in' some 'X-linked recessive inheritance'
DOID:0070599 X-linked spermatogenic failure 8 'has material basis in' some 'X-linked inheritance'
DOID:0070613 familial renal glucosuria 'has material basis in' some 'autosomal dominant inheritance'|'has material basis in' some 'autosomal recessive inheritance'
DOID:0080007 bone deterioration disease 'disease has location' some 'bone element'
DOID:0080010 bone structure disease 'has phenotype' some 'Abnormal bone structure'
DOID:0080020 Jansen's metaphyseal chondrodysplasia 'has material basis in' some 'autosomal dominant inheritance'|'has phenotype' some 'Disproportionate short-limb short stature'
Expand Down Expand Up @@ -3712,7 +3724,7 @@ DOID:0112354 spermatogenic failure 65 'has material basis in' some 'autosomal re
DOID:0112355 spermatogenic failure 60 'has material basis in' some 'autosomal recessive inheritance'
DOID:0112356 spermatogenic failure 63 'has material basis in' some 'autosomal recessive inheritance'
DOID:0112357 spermatogenic failure 59 'has material basis in' some 'autosomal recessive inheritance'
DOID:0112358 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 'has material basis in' some 'autosomal recessive inheritance'
DOID:0112358 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2 'has material basis in' some 'autosomal recessive inheritance'
DOID:0112359 congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay 'has material basis in' some 'autosomal dominant inheritance'
DOID:0112360 spondylocostal dysostosis 6 'has material basis in' some 'autosomal recessive inheritance'
DOID:0112361 spondylocostal dysostosis 3 'has material basis in' some 'autosomal recessive inheritance'
Expand Down Expand Up @@ -3921,6 +3933,7 @@ DOID:11371 functional diarrhea 'has symptom' some diarrhea
DOID:11379 gnathomiasis 'has material basis in' some Gnathostoma|'has symptom' some cough
DOID:11390 cerebral arteritis 'disease has location' some cerebrum
DOID:11394 adult respiratory distress syndrome 'existence starts during' some 'Adult onset'|'has symptom' some shock
DOID:114 heart disease 'disease has location' some 'thoracic segment of trunk'
DOID:11405 diphtheria 'has material basis in' some 'Corynebacterium diphtheriae'|'transmitted by' some ('contact transmission' or 'droplet spread transmission')
DOID:11450 allergic cutaneous vasculitis 'has symptom' some 'allergic reaction'
DOID:11457 brain compression 'has symptom' some abscess
Expand Down Expand Up @@ -4517,6 +4530,7 @@ DOID:3254 bile duct rhabdomyosarcoma 'disease has location' some 'bile duct'
DOID:3261 hyper IgE recurrent infection syndrome 1 'has material basis in' some 'autosomal dominant inheritance'
DOID:3263 piebaldism 'has material basis in' some 'autosomal dominant inheritance'
DOID:3265 chronic granulomatous disease 'has phenotype' some Granuloma
DOID:3277 thymus cancer 'disease has location' some 'thoracic segment of trunk'
DOID:3284 thymic carcinoma 'derives from' some 'epithelial cell'
DOID:3292 mpox 'has symptom' some fever|'has symptom' some headache|'transmitted by' some ('contact transmission' or 'droplet spread transmission' or 'vehicle-borne fomite transmission')
DOID:3298 vaccinia 'has material basis in' some 'Vaccinia virus'|'has symptom' some 'body ache'|'has symptom' some fever|'has symptom' some rash|'transmitted by' some ('contact transmission' or 'vehicle-borne fomite transmission')
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6 changes: 4 additions & 2 deletions DOreports/GARDinDO.tsv
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Expand Up @@ -176,7 +176,7 @@ id label xrefs
"DOID:0050866" "oral squamous cell carcinoma"@en "GARD:7263"
"DOID:0050873" "follicular lymphoma"@en "GARD:2356"
"DOID:0050876" "Caroli disease"@en "GARD:6002"
"DOID:0050877" "pancreatic agenesis"@en "GARD:4203"
"DOID:0050877" "pancreatic agenesis 1"@en "GARD:4203"
"DOID:0050880" "Koolen de Vries syndrome"@en "GARD:10727"
"DOID:0050882" "spinocerebellar ataxia type 5"@en "GARD:4953"
"DOID:0050883" "infantile cerebellar-retinal degeneration"@en "GARD:13264"
Expand Down Expand Up @@ -424,6 +424,8 @@ id label xrefs
"DOID:0060953" "ZTTK syndrome"@en "GARD:13489"
"DOID:0060958" "orofaciodigital syndrome XIV"@en "GARD:13655"
"DOID:0060959" "orofaciodigital syndrome II"@en "GARD:3701"
"DOID:0060986" "preaxial polydactyly II"@en "GARD:5289"
"DOID:0060987" "preaxial polydactyly I"@en "GARD:4417"
"DOID:0070026" "Revesz syndrome"@en "GARD:4695"
"DOID:0070029" "ITM2B-related cerebral amyloid angiopathy 1"@en "GARD:8344"
"DOID:0070055" "Xia-Gibbs Syndrome"@en "GARD:13409"
Expand Down Expand Up @@ -512,6 +514,7 @@ id label xrefs
"DOID:0070561" "glucose transporter type 1 deficiency syndrome 1"@en "GARD:9265"
"DOID:0070562" "Fanconi-Bickel syndrome"@en "GARD:2268"
"DOID:0070563" "glucose-galactose malabsorption"@en "GARD:6521"
"DOID:0070613" "familial renal glucosuria"@en "GARD:7548"
"DOID:0080016" "spina bifida"@en "GARD:7673"
"DOID:0080021" "Schmid metaphyseal chondrodysplasia"@en "GARD:7029"
"DOID:0080028" "spondyloepimetaphyseal dysplasia, Strudwick type"@en "GARD:134"
Expand Down Expand Up @@ -2075,7 +2078,6 @@ id label xrefs
"DOID:9375" "Fuchs' heterochromic uveitis"@en "GARD:6791"
"DOID:9378" "glaucomatocyclitic crisis"@en "GARD:10737"
"DOID:9406" "hypopituitarism"@en "GARD:2917"
"DOID:9432" "renal glycosuria"@en "GARD:7548"
"DOID:9467" "nail-patella syndrome"@en "GARD:7160"
"DOID:9470" "bacterial meningitis"@en "GARD:5881"
"DOID:9476" "Sheehan syndrome"@en "GARD:7630"
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