Update Mondo diff reports (#8564)

Co-authored-by: matentzn <[email protected]>

Author: github-actions[bot]

src/ontology/reports/mondo_base_current_release-report.tsv

@@ -6873,7 +6873,6 @@
 <http://purl.obolibrary.org/obo/MONDO_0005640>	"akinetic mutism"	"A syndrome characterized by a silent and inert state without voluntary motor activity despite preserved sensorimotor pathways and vigilance. Bilateral frontal lobe dysfunction involving the anterior cingulate gyrus and related brain injuries are associated with this condition. This may result in impaired abilities to communicate and initiate motor activities. (From Adams et al., Principles of Neurology, 6th ed, p348; Fortschr Neurol Psychiatr 1995 Feb;63(2):59-67)"	""	
 <http://purl.obolibrary.org/obo/MONDO_0005641>	"aleutian mink disease"	"A slow progressive disease of mink caused by the aleutian mink disease virus. It is characterized by poor reproduction, weight loss, autoimmunity, hypergammaglobulinemia, increased susceptibility to bacterial infections, and death from renal failure. The disease occurs in all color types, but mink which are homozygous recessive for the Aleutian gene for light coat color are particularly susceptible."	""	
 <http://purl.obolibrary.org/obo/MONDO_0700206>	"Parvoviridae infectious disease, non-human animal"	"Parvoviridae infectious disease that occurs in non-human animals."	""	
-<http://purl.obolibrary.org/obo/MONDO_1010029>	"aleutian mink disease, human"	"A human disease caused by infection with Aleutian mink disease parvovirus."	""	
 <http://purl.obolibrary.org/obo/MONDO_0005985>	"Togaviridae infectious disease"	"Virus diseases caused by the togaviridae."	""	
 <http://purl.obolibrary.org/obo/MONDO_0005644>	"amebiasis"	"A parasitic infectious disorder caused by amoebas. The parasite may cause colitis which is manifested with bloody diarrhea, abdominal pain, nausea and fever. In rare cases it may spread to the liver, brain and lungs."	""	
 <http://purl.obolibrary.org/obo/MONDO_0005645>	"ancylostomiasis"	"Infection by hookworms of the genus Ancylostoma."	""	
@@ -6909,7 +6908,6 @@
 <http://purl.obolibrary.org/obo/MONDO_0005676>	"borna disease"	"An encephalomyelitis of horses, sheep and cattle caused by borna disease virus."	""	
 <http://purl.obolibrary.org/obo/MONDO_1011300>	"acute disease, non-human animal"	"Acute disease that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1011327>	"inflammatory disease, non-human animal"	"Inflammatory disease that occurs in non-human animals."	""	
-<http://purl.obolibrary.org/obo/MONDO_0957421>	"borna virus encephalitis"	"A human disease caused by infection with Borna disease virus."	""	
 <http://purl.obolibrary.org/obo/MONDO_0005678>	"bovine respiratory disease complex"	"A multifactorial disease of cattle resulting from complex interactions between environmental factors, host factors, and pathogens. The environmental factors act as stressors adversely affecting the immune system and other host defenses and enhancing transmission of infecting agents."	""	
 <http://purl.obolibrary.org/obo/MONDO_0700104>	"respiratory system disorder, non-human animal"	"Respiratory system disorder that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_0005679>	"bovine virus diarrhea-mucosal disease"	"Acute disease of cattle caused by the bovine viral diarrhea viruses (diarrhea viruses, bovine viral). Often mouth ulcerations are the only sign but fever, diarrhea, drop in milk yield, and loss of appetite are also seen. Severity of clinical disease varies and is strain dependent. Outbreaks are characterized by low morbidity and high mortality."	""	
@@ -10550,6 +10548,7 @@
 <http://purl.obolibrary.org/obo/MONDO_0015229>	"Bardet-Biedl syndrome"	"A ciliopathy with multisystem involvement. It is invariantly characterized by rod-cone dystrophy, and at least three additional non-ocular features such as intellectual disability, obesity, polydactyly, hypogonadism, or renal anomalies as primary manifestations. In the absence of one of these four primary clinical features, the diagnosis of BBS is made when at least two secondary features are observed, including hepatic fibrosis, diabetes mellitus, reproductive and developmental abnormalities, growth retardation, speech delays, or cardiovascular problems"	""	
 <http://purl.obolibrary.org/obo/MONDO_1040043>	"BBS1-related ciliopathy"	"Any ciliopathy caused by variants in the BBS1 gene."	""	
 <http://purl.obolibrary.org/obo/MONDO_0008855>	"MHC class II deficiency"	"Immunodeficiency by defective expression of HLA class 2 is a rare primary genetic immunodeficiency disorder characterized by partial or complete absence of human leukocyte antigen class 2 expression resulting in severe defect in both cellular and humoral immune response to antigens. The disorder presents clinically as marked susceptibility to infections, severe malabsorption and failure to thrive and is often fatal in early childhood."	""	
+<http://purl.obolibrary.org/obo/MONDO_0018814>	"non-SCID combined immunodeficiency"		"True"	
 <http://purl.obolibrary.org/obo/MONDO_0008856>	"immunodeficiency 27A"		""	
 <http://purl.obolibrary.org/obo/MONDO_0019146>	"inherited susceptibility to mycobacterial diseases"	"A rare immunodeficiency syndrome, characterized by a narrow vulnerability to poorly virulent mycobacteria, such as bacillus Calmette-Guerin (BCG) vaccines and environmental mycobacteria (EM), and defined by severe, recurrent infections, either disseminated or localized."	""	
 <http://purl.obolibrary.org/obo/MONDO_0008857>	"Beemer-Ertbruggen syndrome"	"Beemer-Ertbruggen syndrome is a lethal malformation syndrome reported in 2 brothers of first-cousin parents that is characterized by hydrocephalus, cardiac malformation, dense bones, and unusual facies with down-slanting palpebral fissures, bulbous nose, broad nasal bridge, micrognathia and a long upper lip. Transmission is likely autosomal recessive. There have been no further descriptions in the literature since 1984."	""	
@@ -11126,7 +11125,6 @@
 <http://purl.obolibrary.org/obo/MONDO_0009304>	"obsolete Gorlin-Chaudhry-Moss syndrome"		""	"true"
 <http://purl.obolibrary.org/obo/MONDO_0009305>	"granulocytopenia with immunoglobulin abnormality"		""	
 <http://purl.obolibrary.org/obo/MONDO_0009306>	"combined immunodeficiency with skin granulomas"		""	
-<http://purl.obolibrary.org/obo/MONDO_0018814>	"non-SCID combined immunodeficiency"		"True"	
 <http://purl.obolibrary.org/obo/MONDO_0009307>	"granulomatous disease with defect in neutrophil chemotaxis"		""	
 <http://purl.obolibrary.org/obo/MONDO_0018305>	"chronic granulomatous disease"	"Chronic granulomatous disease (CGD) is a rare primary immunodeficiency, mainly affecting phagocytes, which is characterized by an increased susceptibility to severe and recurrent bacterial and fungal infections, along with the development of granulomas."	""	
 <http://purl.obolibrary.org/obo/MONDO_0009308>	"granulomatous disease, chronic, autosomal recessive, cytochrome b-negative"		""	
@@ -26837,6 +26835,7 @@
 <http://purl.obolibrary.org/obo/MONDO_0957403>	"periodic fever syndrome of childhood"		""	
 <http://purl.obolibrary.org/obo/MONDO_0957404>	"obsolete pyogenic autoinflammatory syndrome of childhood"		""	"true"
 <http://purl.obolibrary.org/obo/MONDO_0957405>	"granulomatous autoinflammatory syndrome of childhood"		""	
+<http://purl.obolibrary.org/obo/MONDO_0957421>	"borna virus encephalitis"	"A human disease caused by infection with Borna disease virus."	""	
 <http://purl.obolibrary.org/obo/MONDO_0957423>	"immunotherapy induced hypophysitis"		""	
 <http://purl.obolibrary.org/obo/MONDO_0957426>	"autosomal recessive hyper-IgE syndrome"		"True"	
 <http://purl.obolibrary.org/obo/MONDO_0957427>	"B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)"		""	
@@ -27296,6 +27295,7 @@
 <http://purl.obolibrary.org/obo/MONDO_1010027>	"endocardial fibroelastosis, non-human animal"	"Endocardial fibroelastosis that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010028>	"cerebral amyloid angiopathy, non-human animal"	"Cerebral amyloid angiopathy that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1011415>	"amyloidosis, non-human animal"	"Amyloidosis that occurs in non-human animals."	""	
+<http://purl.obolibrary.org/obo/MONDO_1010029>	"aleutian mink disease, human"	"A human disease caused by infection with Aleutian mink disease parvovirus."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010031>	"triploidy, non-human animal"	"Triploidy that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1011307>	"chromosomal disorder, non-human animal"	"Chromosomal disorder that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010032>	"Jacobsen syndrome, non-human animal"	"Jacobsen syndrome that occurs in non-human animals."	""	
@@ -27498,7 +27498,6 @@
 <http://purl.obolibrary.org/obo/MONDO_1010279>	"hymen, imperforate, non-human animal"	"Hymen, imperforate that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010280>	"priapism, non-human animal"	"Priapism that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010281>	"testicular regression syndrome, non-human animal"	"Testicular regression syndrome that occurs in non-human animals."	""	
-<http://purl.obolibrary.org/obo/MONDO_8000015>	"46,XY sex reversal 11"	"Any 46,XY complete gonadal dysgenesis in which the cause of the disease is a mutation in the DHX37 gene."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010282>	"azoospermia, non-human animal"	"Azoospermia that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010284>	"allergic rhinitis, non-human animal"	"Allergic rhinitis that occurs in non-human animals."	""	
 <http://purl.obolibrary.org/obo/MONDO_1010285>	"atrophic rhinitis, non-human animal"	"Atrophic rhinitis that occurs in non-human animals."	""	
@@ -29887,6 +29886,7 @@
 <http://purl.obolibrary.org/obo/MONDO_8000012>	"neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1"		""	
 <http://purl.obolibrary.org/obo/MONDO_8000013>	"portal hypertension, noncirrhotic, 1"		""	
 <http://purl.obolibrary.org/obo/MONDO_8000014>	"familial antiphospholipid syndrome"	"Autosomal dominant form of antiphospholipid syndrome."	""	
+<http://purl.obolibrary.org/obo/MONDO_8000015>	"46,XY sex reversal 11"	"Any 46,XY complete gonadal dysgenesis in which the cause of the disease is a mutation in the DHX37 gene."	""	
 <http://purl.obolibrary.org/obo/MONDO_8000017>	"obsolete testicular regression syndrome"		""	"true"
 <http://purl.obolibrary.org/obo/MONDO_8000018>	"benign paroxysmal positional vertigo"	"Idiopathic recurrent vertigo associated with positional nystagmus. It is associated with a vestibular loss without other neurological or auditory signs. Unlike in labyrinthitis and vestibular neuronitis inflammation in the ear is not observed."	""	
 <http://purl.obolibrary.org/obo/MONDO_8000019>	"vertigo, benign recurrent, 1"		""