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Remove +/* symbols from DOID:0090101 ICD10CM xrefs
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allenbaron committed Dec 17, 2024
1 parent e5d9310 commit 740a7cd
Showing 1 changed file with 5 additions and 5 deletions.
10 changes: 5 additions & 5 deletions src/ontology/doid-edit.owl
Original file line number Diff line number Diff line change
Expand Up @@ -51463,8 +51463,8 @@ SubClassOf(obo:DOID_0080052 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
# Class: obo:DOID_0080053 (pseudohypoparathyroidism type 1A)

AnnotationAssertion(Annotation(dc:type obo:ECO_0007638) Annotation(oboInOwl:hasDbXref "url:http://en.wikipedia.org/wiki/Albright%27s_hereditary_osteodystrophy") obo:IAO_0000115 obo:DOID_0080053 "A pseudohypoparathyroidism that has_material_basis_in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080053 "MIM:103580")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080053 "GARD:7486")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080053 "MIM:103580")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0080053 "ORDO:79443")
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080053 "Albright hereditary osteodystrophy"@en)
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080053 "Albright's hereditary osteodystrophy"@en)
Expand Down Expand Up @@ -68563,8 +68563,8 @@ SubClassOf(obo:DOID_0090100 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000093
# Class: obo:DOID_0090101 (lethal congenital glycogen storage disease of heart)

AnnotationAssertion(Annotation(dc:type obo:ECO_0007636) Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://ghr.nlm.nih.gov/gene/PRKAG2#conditions") Annotation(oboInOwl:hasDbXref "url:https://www.omim.org/entry/261740") obo:IAO_0000115 obo:DOID_0090101 "A glycogen storage disease characterized by glycogenosis confined to the heart, hypoglycemia and cyanosis, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the gene encoding the noncatalytic gamma-2 subunit of AMP-activated protein kinase (PRKAG2) on chromosome 7q36."@en)
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0090101 "ICD10CM:E74.0+")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0090101 "ICD10CM:G73.6*")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0090101 "ICD10CM:E74.0")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0090101 "ICD10CM:G73.6")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0090101 "MIM:261740")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0090101 "ORDO:439854")
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0090101 "fatal congenital hypertrophic cardiomyopathy due to GSD"@en)
Expand Down Expand Up @@ -201769,12 +201769,13 @@ AnnotationAssertion(oboInOwl:hasAlternativeId obo:DOID_8923 "DOID:10055")
AnnotationAssertion(oboInOwl:hasAlternativeId obo:DOID_8923 "DOID:8922")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "ICD10CM:C43.9")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "ICD9CM:172.9")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "MESH:D000096142")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "MIM:608035")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "MIM:612263")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "NCI:C3510")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "SNOMEDCT_US_2023_03_01:269577007")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "UMLS_CUI:C0151779")
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_8923 "MESH:D000096142")
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "Cutaneous Malignant Melanoma")
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "cutaneous melanoma"@en)
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "malignant ear melanoma"@en)
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "malignant lip melanoma"@en)
Expand All @@ -201787,7 +201788,6 @@ AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "malignant neck melan
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "malignant scalp melanoma"@en)
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "malignant trunk melanoma"@en)
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "malignant upper limb melanoma"@en)
AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_8923 "Cutaneous Malignant Melanoma")
AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_8923 "disease_ontology")
AnnotationAssertion(oboInOwl:id obo:DOID_8923 "DOID:8923")
AnnotationAssertion(oboInOwl:inSubset obo:DOID_8923 doid:DO_cancer_slim)
Expand Down

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