June 2025 release

Author: allenbaron

DOreports/DO-subClassOf-anonymous.tsv

@@ -156,7 +156,7 @@ DOID:0050198	Chapare hemorrhagic fever	'has material basis in' some 'Mammarenavi
 DOID:0050199	Whitewater Arroyo hemorrhagic fever	'has material basis in' some 'Mammarenavirus whitewaterense'|'has symptom' some fever|'has symptom' some headache|'has symptom' some hemorrhage|'transmitted by' some 'Neotoma albigula'
 DOID:0050200	Korean hemorrhagic fever	'has symptom' some 'abdominal pain'|'has symptom' some 'bloodshot eye'|'has symptom' some 'low blood pressure'|'has symptom' some backache|'has symptom' some chills|'has symptom' some fever|'has symptom' some flushing|'has symptom' some headache|'has symptom' some hypotension|'has symptom' some nausea|'has symptom' some rash|'has symptom' some shock|'transmitted by' some ('Rattus norvegicus' or 'Apodemus agrarius')
 DOID:0050201	nephropathia epidemica	'has material basis in' some 'Orthohantavirus puumalaense'|'has symptom' some 'abdominal pain'|'has symptom' some 'renal failure'|'has symptom' some backache|'has symptom' some headache|'has symptom' some hemorrhage|'has symptom' some nausea|'has symptom' some vomiting|'transmitted by' some 'Myodes glareolus'
-DOID:0050202	Lujo hemorrhagic fever	'has material basis in' some 'Mammarenavirus lujoense'|'has symptom' some bleeding
+DOID:0050202	Lujo hemorrhagic fever	'has material basis in' some 'Mammarenavirus lujoense'|'has symptom' some 'muscle pain'|'has symptom' some bleeding|'has symptom' some fever|'has symptom' some headache|'has symptom' some thrombocytopenia
 DOID:0050204	Epstein-Barr virus hepatitis	'has material basis in' some 'Lymphocryptovirus humangamma4'|'has symptom' some 'abdominal pain'|'has symptom' some 'liver inflammation'|'has symptom' some fatigue|'has symptom' some fever|'has symptom' some headache|'has symptom' some jaundice|'has symptom' some nausea
 DOID:0050211	swine influenza	'has symptom' some 'pharynx inflammation'|'has symptom' some cough|'has symptom' some diarrhea|'has symptom' some fever|'has symptom' some lethargy|'has symptom' some nausea|'has symptom' some rhinorrhea|'has symptom' some vomiting|('has material basis in' some 'Alphainfluenzavirus influenzae') or ('has material basis in' some 'Gammainfluenzavirus influenzae')
 DOID:0050214	Lambert-Eaton myasthenic syndrome	'has phenotype' some 'Abnormal circulating immunoglobulin concentration'
@@ -233,6 +233,7 @@ DOID:0050488	early congenital syphilis	'disease has basis in' some 'Abnormality
 DOID:0050490	parenchymatous neurosyphilis	'has symptom' some 'concentration difficulty'|'has symptom' some fatigue|'has symptom' some headache|'has symptom' some insomnia|'has symptom' some irritability|'has symptom' some lethargy
 DOID:0050491	meningovascular neurosyphilis	'disease has feature' some 'muscular atrophy'|'has symptom' some 'memory impairment'|'has symptom' some 'memory loss'|'has symptom' some 'muscle weakness'|'has symptom' some 'stiff neck'|'has symptom' some 'urinary incontinence'|'has symptom' some dizziness|'has symptom' some headache|'has symptom' some insomnia|'has symptom' some paralysis
 DOID:0050495	exanthema subitum	'has symptom' some 'high fever'|('has material basis in' some 'Human betaherpesvirus 6') or ('has material basis in' some 'Roseolovirus humanbeta6b') or ('has material basis in' some 'Roseolovirus humanbeta7')
+DOID:0050508	variola major	'has material basis in' some 'Variola virus'
 DOID:0050513	spinal polio	'disease has location' some 'spinal cord'|'has symptom' some 'breathing problems'|'has symptom' some 'hind limb paralysis'
 DOID:0050514	bulbospinal polio	'disease has location' some ('spinal cord' or brainstem)|'has symptom' some 'breathing problems'|'has symptom' some 'hind limb paralysis'|'has symptom' some dysphagia|'has symptom' some paralysis
 DOID:0050515	paralytic poliomyelitis	'disease has location' some 'central nervous system'|'has symptom' some 'flaccid paralysis'
@@ -993,7 +994,7 @@ DOID:0061045	autosomal dominant intellectual developmental disorder 72	'has mate
 DOID:0061046	autosomal dominant intellectual developmental disorder 73	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0061047	autosomal dominant intellectual developmental disorder 74	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0061048	autosomal dominant intellectual developmental disorder 75	'has material basis in' some 'autosomal dominant inheritance'
-DOID:0061049	autosomal dominant intellectual developmental disorder  type FRA12A	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0061049	autosomal dominant intellectual developmental disorder type FRA12A	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0061051	immunodeficiency 80	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0061052	immunodeficiency 81	'existence starts during' some 'Infantile onset'|'has material basis in' some 'autosomal recessive inheritance'
 DOID:0061053	immunodeficiency 82	'has material basis in' some 'autosomal dominant inheritance'
@@ -1079,8 +1080,15 @@ DOID:0061141	complex cortical dysplasia with other brain malformations 12	'has m
 DOID:0061142	complex cortical dysplasia with other brain malformations 11	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0061143	complex cortical dysplasia with other brain malformations 10	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0061144	complex cortical dysplasia with other brain malformations 13	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0061145	monilethrix 1	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0061146	Pan-Chung-Bellen syndrome	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0061147	neurodevelopmental disorder with or without autism or seizures	'disease has basis in' some symptom|'has material basis in' some 'autosomal dominant inheritance'
+DOID:0061148	hereditary congenital ptosis 2	'disease has basis in' some 'Abnormality of prenatal development or birth'|'has material basis in' some 'X-linked recessive inheritance'
+DOID:0061149	hereditary congenital ptosis 1	'disease has basis in' some 'Abnormality of prenatal development or birth'|'has material basis in' some 'autosomal dominant inheritance'
+DOID:0061150	familial isolated hypoparathyroidism 1	'has material basis in' some 'autosomal dominant inheritance'|'has material basis in' some 'autosomal recessive inheritance'
+DOID:0061151	familial isolated hypoparathyroidism 2	'has material basis in' some 'autosomal dominant inheritance'|'has material basis in' some 'autosomal recessive inheritance'
+DOID:0061152	monilethrix 2	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0061153	monilethrix 3	'has material basis in' some 'autosomal dominant 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:0070013	Seckel syndrome 2	'has material basis in' some 'autosomal recessive inheritance'
@@ -1465,6 +1473,11 @@ DOID:0070615	autoinflammation, antibody deficiency, and immune dysregulation syn
 DOID:0070617	rhabdoid tumor predisposition syndrome	'existence starts during' some ('Infantile onset' or 'Childhood onset')|'has material basis in' some 'autosomal dominant inheritance'
 DOID:0070618	rhabdoid tumor predisposition syndrome 1	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0070629	acute myeloid leukemia with CBFA2T3-GLIS2 fusion	'existence starts during' some ('Infantile onset' or 'Childhood onset')
+DOID:0070636	mirror movements 1	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0070637	mirror movements 2	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0070638	mirror movements 4	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0070639	mirror movements 3	'has material basis in' some 'autosomal recessive inheritance'
+DOID:0070644	hereditary spastic paraplegia 92	'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'
@@ -1509,7 +1522,7 @@ DOID:0080087	nonsyndromic congenital nail disorder 9	'disease has basis in' some
 DOID:0080089	tubular aggregate myopathy 1	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0080090	reducing body myopathy 1A	'has material basis in' some 'X-linked dominant inheritance'
 DOID:0080092	myofibrillar myopathy 1	'has material basis in' some 'autosomal dominant inheritance'|'has material basis in' some 'autosomal recessive inheritance'
-DOID:0080093	myofibrillar myopathy 2	'has material basis in' some 'autosomal dominant inheritance'
+DOID:0080093	adult-onset myofibrillar myopathy 2A	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0080094	myofibrillar myopathy 3	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0080095	myofibrillar myopathy 4	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0080096	myofibrillar myopathy 5	'has material basis in' some 'autosomal dominant inheritance'
@@ -1624,7 +1637,7 @@ DOID:0080303	mucinous lung adenocarcinoma	'derives from' some ('epithelial cell'
 DOID:0080304	lung mucinous cystadenocarcinoma	'derives from' some 'glandular secretory epithelial cell'
 DOID:0080307	myofibrillar myopathy	'has symptom' some 'muscle weakness'|'has symptom' some 'progressive weakness'
 DOID:0080308	myofibrillar myopathy 8	'has material basis in' some 'autosomal recessive inheritance'|'has symptom' some 'muscle weakness'|'has symptom' some 'progressive weakness'
-DOID:0080309	fatal infantile hypertonic myofibrillar myopathy	'has material basis in' some 'autosomal recessive inheritance'
+DOID:0080309	infantile-onset myofibrillar myopathy-2B	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0080312	neurodevelopmental disorder with midbrain and hindbrain malformations	'has material basis in' some 'autosomal recessive inheritance'|'has phenotype' some 'Neurodevelopmental delay'
 DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1	'has material basis in' some 'autosomal recessive inheritance'
 DOID:0080317	megalencephalic leukoencephalopathy with subcortical cysts 2B	'has material basis in' some 'autosomal dominant inheritance'
@@ -2057,7 +2070,6 @@ DOID:0081114	benign familial infantile seizures 1	'has material basis in' some '
 DOID:0081115	benign familial infantile seizures 2	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0081116	benign familial infantile seizures 3	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0081118	benign familial infantile seizures 5	'has material basis in' some 'autosomal dominant inheritance'
-DOID:0081119	benign familial infantile seizures 6	'has material basis in' some 'autosomal dominant inheritance'
 DOID:0081121	inclusion body myopathy and brain white matter abnormalities	'existence starts during' some 'Adult onset'|'has material basis in' some 'autosomal dominant inheritance'
 DOID:0081123	X-linked mental retardation Gustavson type	'existence starts during' some 'Infantile onset'|'has material basis in' some 'X-linked inheritance'
 DOID:0081124	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1	'has material basis in' some 'autosomal recessive inheritance'
@@ -5587,6 +5599,7 @@ DOID:9111	cutaneous leishmaniasis	'disease has location' some 'zone of skin'
 DOID:9113	granuloma inguinale	'has material basis in' some 'Klebsiella granulomatis'|'transmitted by' some 'contact transmission'
 DOID:9123	eczema herpeticum	'disease has location' some 'zone of skin'|'has symptom' some 'lymph gland swelling'|'has symptom' some fever|('has material basis in' some 'Simplexvirus humanalpha1') or ('has material basis in' some 'Simplexvirus humanalpha2')
 DOID:9146	visceral leishmaniasis	'disease has location' some 'bone element'|'disease has location' some liver|'disease has location' some spleen|'has symptom' some 'weight loss'|'has symptom' some fever|'has symptom' some hepatomegaly|'has symptom' some splenomegaly
+DOID:9153	variola minor	'has material basis in' some 'Variola virus'
 DOID:9155	mucocutaneous leishmaniasis	'disease has location' some 'upper respiratory tract'
 DOID:9159	gas gangrene	'disease has feature' some 'bacterial sepsis'|'has material basis in' some 'Clostridium perfringens'|'has symptom' some blister|'has symptom' some gangrene|'has symptom' some necrosis
 DOID:9169	Wiskott-Aldrich syndrome	'has material basis in' some 'X-linked recessive inheritance'

DOreports/GARDinDO.tsv

@@ -932,6 +932,7 @@ id	label	xrefs
 "DOID:0111146"	"acquired von Willebrand syndrome"	"GARD:5573"
 "DOID:0111147"	"angioimmunoblastic T-cell lymphoma"	"GARD:11973"
 "DOID:0111152"	"multicentric Castleman disease"	"GARD:9644"
+"DOID:0111153"	"congenital mirror movement disorder"	"GARD:12551"
 "DOID:0111154"	"postural orthostatic tachycardia syndrome"	"GARD:9597"
 "DOID:0111156"	"spermatogenic failure 9"	"GARD:12502"
 "DOID:0111157"	"Castleman disease"	"GARD:12656"
@@ -997,6 +998,7 @@ id	label	xrefs
 "DOID:0111381"	"IVIC syndrome"	"GARD:269"
 "DOID:0111382"	"ischiocoxopodopatellar syndrome"	"GARD:3030"
 "DOID:0111383"	"autosomal dominant keratitis"	"GARD:3089"
+"DOID:0111387"	"familial isolated hypoparathyroidism"	"GARD:2910"
 "DOID:0111389"	"mucopolysaccharidosis Ih/s"	"GARD:12560"
 "DOID:0111390"	"mucopolysaccharidosis Ih"	"GARD:12559"
 "DOID:0111391"	"mucopolysaccharidosis IVA"	"GARD:3785"