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Synonym Sync - Redundant whitespace - mini build
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joeflack4 committed Dec 24, 2024
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2 changes: 0 additions & 2 deletions src/ontology/reports/sync-synonym/doid.synonyms.added.robot.tsv
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Expand Up @@ -4038,7 +4038,6 @@ MONDO:0010517 ciliary dyskinesia, primary, 36, X-linked oio:hasExactSynonym X-l
MONDO:0010517 ciliary dyskinesia, primary, 36, X-linked oio:hasExactSynonym primary ciliary dyskinesia 36 DOID:0111850 primary ciliary dyskinesia 36 primary ciliary dyskinesia 36 DOID:0111850
MONDO:0010521 amelogenesis imperfecta type 1E oio:hasExactSynonym amelogenesis imperfecta type 1E DOID:0110058 amelogenesis imperfecta type 1E amelogenesis imperfecta type 1E DOID:0110058
MONDO:0010522 X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 oio:hasExactSynonym X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 DOID:0110059 X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 DOID:0110059
MONDO:0010522 X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 oio:hasExactSynonym amelogenesis imperfecta type IE X-linked 2 DOID:0110059 X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 amelogenesis imperfecta type IE X-linked 2 DOID:0110059
MONDO:0010523 X-linked reticulate pigmentary disorder oio:hasExactSynonym X-linked reticulate pigmentary disorder DOID:0111834 X-linked reticulate pigmentary disorder X-linked reticulate pigmentary disorder DOID:0111834
MONDO:0010523 X-linked reticulate pigmentary disorder oio:hasExactSynonym X-linked reticulate pigmentary disorder with systemic manifestations DOID:0111834 X-linked reticulate pigmentary disorder X-linked reticulate pigmentary disorder with systemic manifestations DOID:0111834
MONDO:0010524 X-linked sideroblastic anemia with ataxia oio:hasExactSynonym Anemia, sideroblastic, spinocerebellar ataxia DOID:0050554 X-linked sideroblastic anemia with ataxia Anemia, sideroblastic, spinocerebellar ataxia DOID:0050554
Expand Down Expand Up @@ -4367,7 +4366,6 @@ MONDO:0011362 myopathy, myofibrillar, 9, with early respiratory failure oio:hasE
MONDO:0011362 myopathy, myofibrillar, 9, with early respiratory failure oio:hasExactSynonym proximal myopathy with early respiratory muscle involvement DOID:0111188 myofibrillar myopathy 9 proximal myopathy with early respiratory muscle involvement DOID:0111188
MONDO:0011362 myopathy, myofibrillar, 9, with early respiratory failure oio:hasExactSynonym MFM9 DOID:0111188 myofibrillar myopathy 9 http://purl.obolibrary.org/obo/mondo#ABBREVIATION MFM9 DOID:0111188 http://purl.obolibrary.org/obo/mondo#ABBREVIATION
MONDO:0011362 myopathy, myofibrillar, 9, with early respiratory failure oio:hasExactSynonym MPRM DOID:0111188 myofibrillar myopathy 9 http://purl.obolibrary.org/obo/mondo#ABBREVIATION MPRM DOID:0111188 http://purl.obolibrary.org/obo/mondo#ABBREVIATION
MONDO:0011365 blepharophimosis - intellectual disability syndrome, SBBYS type oio:hasExactSynonym Ohdo syndrome, SBBYS variant DOID:0060290 Ohdo syndrome, SBBYS variant Ohdo syndrome, SBBYS variant DOID:0060290
MONDO:0011365 blepharophimosis - intellectual disability syndrome, SBBYS type oio:hasExactSynonym blepharophimosis-intellectual disability syndrome, SBBYS type DOID:0060290 Ohdo syndrome, SBBYS variant blepharophimosis-intellectual disability syndrome, SBBYS type DOID:0060290
MONDO:0011374 hypercholesterolemia, familial, 4 oio:hasExactSynonym autosomal recessive hypercholesterolemia DOID:0090105 autosomal recessive hypercholesterolemia autosomal recessive hypercholesterolemia DOID:0090105
MONDO:0011381 dominant beta-thalassemia oio:hasExactSynonym autosomal dominant beta thalassemia DOID:0080770 autosomal dominant beta thalassemia autosomal dominant beta thalassemia DOID:0080770
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16 changes: 9 additions & 7 deletions src/ontology/reports/sync-synonym/doid.synonyms.confirmed.robot.tsv
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2 changes: 1 addition & 1 deletion src/ontology/reports/sync-synonym/doid.synonyms.updated.robot.tsv
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Expand Up @@ -2168,8 +2168,8 @@ MONDO:0010294 X-linked severe congenital neutropenia oio:hasExactSynonym oio:has
MONDO:0010298 Lesch-Nyhan syndrome oio:hasExactSynonym oio:hasRelatedSynonym Hprt1 deficiency Hprt1 deficiency HPRT1 deficiency DOID:1919 Lesch-Nyhan syndrome Hprt1 deficiency DOID:1919
MONDO:0010299 hypoxanthine guanine phosphoribosyltransferase partial deficiency oio:hasExactSynonym oio:hasRelatedSynonym KELLEY-Seegmiller syndrome KELLEY-Seegmiller syndrome Kelley-Seegmiller syndrome DOID:0112127 HRPT-related hyperuricemia KELLEY-Seegmiller syndrome DOID:0112127
MONDO:0010302 Ito hypomelanosis oio:hasExactSynonym oio:hasRelatedSynonym Incontinentia pigmenti achromians Incontinentia pigmenti achromians incontinentia pigmenti achromians DOID:3156 hypomelanosis of Ito Incontinentia pigmenti achromians DOID:3156
MONDO:0010306 X-linked intellectual disability, Cabezas type oio:hasExactSynonym oio:hasRelatedSynonym mental retardation, X-linked, syndromic 15 DOID:0060822 syndromic X-linked intellectual disability Cabezas type http://purl.obolibrary.org/obo/mondo#DEPRECATED mental retardation, X-linked, syndromic 15 DOID:0060822
MONDO:0010306 X-linked intellectual disability, Cabezas type oio:hasExactSynonym oio:hasRelatedSynonym mental retardation, X-linked, syndromic 15 mental retardation, X-linked, syndromic 15 mental retardation, x-linked, syndromic 15 DOID:0060822 syndromic X-linked intellectual disability Cabezas type http://purl.obolibrary.org/obo/mondo#DEPRECATED mental retardation, X-linked, syndromic 15 DOID:0060822
MONDO:0010306 X-linked intellectual disability, Cabezas type oio:hasExactSynonym oio:hasRelatedSynonym mental retardation, X-linked, syndromic 15 DOID:0060822 syndromic X-linked intellectual disability Cabezas type http://purl.obolibrary.org/obo/mondo#DEPRECATED mental retardation, X-linked, syndromic 15 DOID:0060822
MONDO:0010313 intellectual disability, X-linked 63 oio:hasExactSynonym oio:hasRelatedSynonym ACSL4-related intellectual disability DOID:0112050 non-syndromic X-linked intellectual disability 63 GARD:0005613 ACSL4-related intellectual disability DOID:0112050
MONDO:0010313 intellectual disability, X-linked 63 oio:hasExactSynonym oio:hasRelatedSynonym MRX63 DOID:0112050 non-syndromic X-linked intellectual disability 63 http://purl.obolibrary.org/obo/mondo#ABBREVIATION http://purl.obolibrary.org/obo/mondo#DEPRECATED MONDO:Lexical MRX63 DOID:0112050 http://purl.obolibrary.org/obo/mondo#ABBREVIATION
MONDO:0010317 intellectual disability, X-linked, with or without seizures, arx-related oio:hasExactSynonym oio:hasRelatedSynonym ARX-related intellectual disability DOID:0112021 non-syndromic X-linked intellectual disability ARX-related GARD:0005614 ARX-related intellectual disability DOID:0112021
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2 changes: 1 addition & 1 deletion src/ontology/reports/sync-synonym/icd10cm.synonyms.updated.robot.tsv
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Expand Up @@ -48,8 +48,8 @@ MONDO:0006702 chronic inflammatory demyelinating polyradiculoneuropathy oio:hasE
MONDO:0006861 myeloid sarcoma oio:hasExactSynonym oio:hasRelatedSynonym granulocytic sarcoma granulocytic sarcoma Granulocytic sarcoma ICD10CM:C92.3 Myeloid sarcoma granulocytic sarcoma ICD10CM:C92.3
MONDO:0007039 NF2-related schwannomatosis oio:hasExactSynonym oio:hasBroadSynonym acoustic neurofibromatosis acoustic neurofibromatosis Acoustic neurofibromatosis ICD10CM:Q85.02 Neurofibromatosis, type 2 acoustic neurofibromatosis ICD10CM:Q85.02
MONDO:0007039 NF2-related schwannomatosis oio:hasExactSynonym oio:hasRelatedSynonym neurofibromatosis, type 2 neurofibromatosis, type 2 Neurofibromatosis, type 2 ICD10CM:Q85.02 Neurofibromatosis, type 2 neurofibromatosis, type 2 ICD10CM:Q85.02
MONDO:0007345 aorta coarctation oio:hasExactSynonym oio:hasRelatedSynonym coarctation of aorta ICD10CM:Q25.1 Coarctation of aorta coarctation of aorta ICD10CM:Q25.1
MONDO:0007345 aorta coarctation oio:hasExactSynonym oio:hasRelatedSynonym coarctation of aorta coarctation of aorta Coarctation of aorta ICD10CM:Q25.1 Coarctation of aorta coarctation of aorta ICD10CM:Q25.1
MONDO:0007345 aorta coarctation oio:hasExactSynonym oio:hasRelatedSynonym coarctation of aorta ICD10CM:Q25.1 Coarctation of aorta coarctation of aorta ICD10CM:Q25.1
MONDO:0007699 Hashimoto thyroiditis oio:hasExactSynonym oio:hasRelatedSynonym autoimmune thyroiditis autoimmune thyroiditis Autoimmune thyroiditis ICD10CM:E06.3 Autoimmune thyroiditis autoimmune thyroiditis ICD10CM:E06.3
MONDO:0007699 Hashimoto thyroiditis oio:hasExactSynonym oio:hasBroadSynonym lymphocytic thyroiditis lymphocytic thyroiditis Lymphocytic thyroiditis ICD10CM:E06.3 Autoimmune thyroiditis lymphocytic thyroiditis ICD10CM:E06.3
MONDO:0007810 autosomal dominant ichthyosis vulgaris oio:hasExactSynonym oio:hasRelatedSynonym ichthyosis vulgaris ichthyosis vulgaris Ichthyosis vulgaris ICD10CM:Q80.0 Ichthyosis vulgaris ichthyosis vulgaris ICD10CM:Q80.0
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