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update due to QC failures
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@katiermullen
katiermullen committed Jan 29, 2025
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Showing 1 changed file with 17 additions and 3 deletions.
20 changes: 17 additions & 3 deletions src/ontology/mondo-edit.obo
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Expand Up @@ -588537,6 +588537,7 @@ name: von Willebrand disease III, domestic cat
def: "Any von Willebrand disease that occurs in cats and is characterized by no detectable or a severe quantitative deficiency of the glycoprotein von Willebrand factor (vWF)." [OMIA:001058-9685]
xref: OMIA:001058-9685 {source="MONDO:equivalentTo"}
is_a: MONDO:1011613 {source="OMIA:001058-9685", source="https://orcid.org/0000-0002-5002-8648"} ! Von Willebrand disease, domestic cat
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: in_taxon NCBITaxon:9685 {source="OMIA:001058-9685"} ! Felis catus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI

Expand Down Expand Up @@ -588601,6 +588602,7 @@ xref: OMIA:001179-9615 {source="MONDO:equivalentTo"}
is_a: MONDO:1012109 {source="OMIA:001179-9615", source="https://orcid.org/0000-0002-5002-8648"} ! hypoadrenocorticism, dog
is_a: MONDO:1012121 {source="OMIA:001179-9615", source="https://orcid.org/0000-0002-5002-8648"} ! primary hypothyroidism, dog
is_a: MONDO:1012985 {source="OMIA:001179-9615", source="https://orcid.org/0000-0002-5002-8648"} ! autoimmune disease, non-human animal
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: in_taxon NCBITaxon:9615 {source="OMIA:001179-9615"} ! Canis lupus familiaris
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI

Expand Down Expand Up @@ -588788,6 +588790,7 @@ name: von Willebrand disease II, horse
def: "Any von Willebrand disease that occurs in horses and is characterized by qualitative abnormalities of the glycoprotein von Willebrand factor (vWF) and moderate to severe bleeding." [OMIA:001339-9796]
xref: OMIA:001339-9796 {source="MONDO:equivalentTo"}
is_a: MONDO:1011614 {source="OMIA:001339-9796", source="https://orcid.org/0000-0002-5002-8648"} ! Von Willebrand disease, horse
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: in_taxon NCBITaxon:9796 {source="OMIA:001339-9796"} ! Equus caballus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI

Expand Down Expand Up @@ -588897,6 +588900,7 @@ synonym: "Waardenburg syndrome, type 2A, golden hamster" RELATED [OMIA:001401-10
xref: OMIA:001401-10036 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:001401-10036", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
is_a: MONDO:1011618 {source="OMIA:001401-10036", source="https://orcid.org/0000-0002-5002-8648"} ! Waardenburg syndrome, golden hamster
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/101823465 {source="OMIA:001401-10036", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:10036 {source="OMIA:001401-10036"} ! Mesocricetus auratus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -589133,6 +589137,7 @@ name: demyelinating disorder, Limousin cattle
def: "Any demyelinating disease that occurs in calves of the Limousin breed of cattle and is characterized by progressively severe forelimb hypermetria, blindness, behavioural abnormalities and multifocal white matter vacuolation and demyelination." [PMID:2375709]
xref: OMIA:001489-9913 {source="MONDO:equivalentTo"}
is_a: MONDO:1012987 {source="OMIA:001489-9913", source="https://orcid.org/0000-0002-5002-8648"} ! demyelinating disease, non-human animal
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: in_taxon NCBITaxon:9913 {source="OMIA:001489-9913"} ! Bos taurus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI

Expand Down Expand Up @@ -589213,7 +589218,7 @@ property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/
[Term]
id: MONDO:1012704
name: oculoskeletal dysplasia, COL9A3-related, dog
def: "Any retinal and skeletal dysplasia that occurs in dogs due to a mutation in the COL9A3 gene. " [MONDO:patterns/nonhuman_disease_series_by_gene]
def: "Any retinal and skeletal dysplasia that occurs in dogs due to a mutation in the COL9A3 gene." [MONDO:patterns/nonhuman_disease_series_by_gene]
synonym: "oculoskeletal dysplasia 1, dog" RELATED [OMIA:001522-9615]
xref: OMIA:001522-9615 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:001522-9615", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
Expand All @@ -589226,7 +589231,7 @@ property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/
[Term]
id: MONDO:1012705
name: oculoskeletal dysplasia, COL9A2-related, dog
def: "Any retinal and skeletal dysplasia that occurs in dogs due to a mutation in the COL9A2 gene. " [MONDO:patterns/nonhuman_disease_series_by_gene]
def: "Any retinal and skeletal dysplasia that occurs in dogs due to a mutation in the COL9A2 gene." [MONDO:patterns/nonhuman_disease_series_by_gene]
synonym: "oculoskeletal dysplasia 2, dog" RELATED [OMIA:001523-9615]
xref: OMIA:001523-9615 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:001523-9615", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
Expand Down Expand Up @@ -589370,6 +589375,7 @@ name: early-onset retinal dystrophy, Bengal, domestic cat
def: "Any retinal dystrophy that occurs in the Bengal breed of domestic cats characterized as early-onset primary photoreceptor disorder that leads to blindness within the first year of age." [PMID:21923821]
xref: OMIA:001613-9685 {source="MONDO:equivalentTo"}
is_a: MONDO:1012243 {source="OMIA:001613-9685", source="https://orcid.org/0000-0002-5002-8648"} ! retinal dystrophy, domestic cat
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: in_taxon NCBITaxon:9685 {source="OMIA:001613-9685"} ! Felis catus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI

Expand Down Expand Up @@ -589415,6 +589421,7 @@ synonym: "retinal atrophy-rod-cone dysplasia 1a, dog" RELATED [OMIA:001669-9615]
xref: OMIA:001669-9615 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:001669-9615", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
is_a: MONDO:1012630 {source="OMIA:001669-9615", source="https://orcid.org/0000-0002-5002-8648"} ! rod-cone dysplasia 1, PDE6B-related, dog
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/399653 {source="OMIA:001669-9615", source="https://orcid.org/0000-0002-5002-8648"} ! PDE6B
relationship: in_taxon NCBITaxon:9615 {source="OMIA:001669-9615"} ! Canis lupus familiaris
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -590178,6 +590185,7 @@ def: "Any neuroaxonal dystrophy that occurs in sheep due to a mutation in the PL
xref: OMIA:002105-9940 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:002105-9940", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
is_a: MONDO:1011565 {source="OMIA:002105-9940", source="https://orcid.org/0000-0002-5002-8648"} ! neuroaxonal dystrophy, sheep
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/101103799 {source="OMIA:002105-9940", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:9940 {source="OMIA:002105-9940"} ! Ovis aries
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -590298,6 +590306,7 @@ synonym: "osteogenesis imperfecta, type II, COL1A1-related, cattle" EXACT [OMIA:
xref: OMIA:002127-9913 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:002127-9913", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
is_a: MONDO:1011580 {source="OMIA:002127-9913", source="https://orcid.org/0000-0002-5002-8648"} ! osteogenesis imperfecta, cattle
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/282187 {source="OMIA:002127-9913", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:9913 {source="OMIA:002127-9913"} ! Bos taurus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -590678,6 +590687,7 @@ synonym: "inherited retinal dystrophic or degenerative disorders, domestic cat"
xref: OMIA:002267-9685 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:002267-9685", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
is_a: MONDO:1012227 {source="OMIA:002267-9685", source="https://orcid.org/0000-0002-5002-8648"} ! progressive retinal atrophy, domestic cat
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/101094089 {source="OMIA:002267-9685", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:9685 {source="OMIA:002267-9685"} ! Felis catus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -591080,6 +591090,7 @@ def: "Any retinal dysplasia that occurs in dogs due to a mutation in the NDP gen
xref: OMIA:002348-9615 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:002348-9615", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
is_a: MONDO:1012241 {source="OMIA:002348-9615", source="https://orcid.org/0000-0002-5002-8648"} ! retinal dysplasia, dog
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/612440 {source="OMIA:002348-9615", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:9615 {source="OMIA:002348-9615"} ! Canis lupus familiaris
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -591243,6 +591254,7 @@ def: "Any spinal muscular atrophy that occurs in domestic cats due to a mutation
xref: OMIA:002389-9685 {source="MONDO:equivalentTo"}
is_a: MONDO:1010996 {source="OMIA:002389-9685", source="https://orcid.org/0000-0002-5002-8648"} ! spinal muscular atrophy, domestic cat
is_a: MONDO:1011321 {source="OMIA:002389-9685", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/751823 {source="OMIA:002389-9685", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:9685 {source="OMIA:002389-9685"} ! Felis catus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -591599,6 +591611,7 @@ def: "Any osteogenesis imperfecta that occurs in domestic cats due to a mutation
xref: OMIA:002533-9685 {source="MONDO:equivalentTo"}
is_a: MONDO:1011321 {source="OMIA:002533-9685", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
is_a: MONDO:1011582 {source="OMIA:002533-9685", source="https://orcid.org/0000-0002-5002-8648"} ! osteogenesis imperfecta, domestic cat
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/101087097 {source="OMIA:002533-9685", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:9685 {source="OMIA:002533-9685"} ! Felis catus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down Expand Up @@ -591771,10 +591784,11 @@ property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/
[Term]
id: MONDO:1012936
name: persistent truncus arteriosus, GATA6-related, cattle
def: "Any persistent truncus arteriosus that occurs in cattle due to a mutation in the GATA6 gene." [MONDO:patterns/nonhuman_disease_series_by_gene]
def: "Any persistent truncus arteriosus that occurs in cattle due to a mutation in the GATA6 gene." [MONDO:patterns/nonhuman_disease_series_by_gene]
xref: OMIA:002559-9913 {source="MONDO:equivalentTo"}
is_a: MONDO:1010475 {source="OMIA:002559-9913", source="https://orcid.org/0000-0002-5002-8648"} ! persistent truncus arteriosus, cattle
is_a: MONDO:1011321 {source="OMIA:002559-9913", source="https://orcid.org/0000-0002-5002-8648"} ! hereditary disease, non-human animal
relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
relationship: has_material_basis_in_germline_mutation_in http://identifiers.org/ncbigene/654400 {source="OMIA:002559-9913", source="https://orcid.org/0000-0002-5002-8648"}
relationship: in_taxon NCBITaxon:9913 {source="OMIA:002559-9913"} ! Bos taurus
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7271" xsd:anyURI
Expand Down

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