Update slurp/omim.tsv

Updated file directly without running any prerequisites. Proof of bugfix on slurp following previous commit.
monarch-initiative · Mar 21, 2024 · 86b4abf · 86b4abf
1 parent ac9c70d
commit 86b4abf
Showing 1 changed file with 8 additions and 20 deletions.
diff --git a/src/ontology/slurp/omim.tsv b/src/ontology/slurp/omim.tsv
@@ -2,25 +2,13 @@ mondo_id	mondo_label	xref	xref_source	original_label	definition	parents
 ID	LABEL	A oboInOwl:hasDbXref	>A oboInOwl:source SPLIT=|		A IAO:0000115	SC %
 MONDO:0958222	maple syrup urine disease,  iia 1b	OMIM:620698	MONDO:equivalentTo	maple syrup urine disease,  iia 1b		
 MONDO:0958223	maple syrup urine disease,  iia 2	OMIM:620699	MONDO:equivalentTo	maple syrup urine disease,  iia 2		
-MONDO:0958224	encephalopathy, porphyria-related	OMIM:620704	MONDO:equivalentTo	encephalopathy, porphyria-related		
-MONDO:0958225	epidermolytic hyperkeratosis 2b, autosomal recessive	OMIM:620707	MONDO:equivalentTo	epidermolytic hyperkeratosis 2b, autosomal recessive		
-MONDO:0958226	leukoencephalopathy, porphyria-related	OMIM:620711	MONDO:equivalentTo	leukoencephalopathy, porphyria-related		
+MONDO:0958225	epidermolytic hyperkeratosis 2b, autosomal recessive	OMIM:620707	MONDO:equivalentTo	epidermolytic hyperkeratosis 2b, autosomal recessive		MONDO:0957316
 MONDO:0958227	polydactyly-macrocephaly syndrome	OMIM:620712	MONDO:equivalentTo	polydactyly-macrocephaly syndrome		
-MONDO:0958228	deafness, autosomal recessive 122	OMIM:620714	MONDO:equivalentTo	deafness, autosomal recessive 122		
+MONDO:0958228	deafness, autosomal recessive 122	OMIM:620714	MONDO:equivalentTo	deafness, autosomal recessive 122		MONDO:0019588
 MONDO:0958229	bleeding disorder, vascular-type	OMIM:620715	MONDO:equivalentTo	bleeding disorder, vascular-type		
-MONDO:0958230	orofaciodigital syndrome 20	OMIM:620718	MONDO:equivalentTo	orofaciodigital syndrome 20		
-MONDO:0958231	neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism	OMIM:620719	MONDO:equivalentTo	neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism		
-MONDO:0958232	deafness, autosomal dominant 90	OMIM:620722	MONDO:equivalentTo	deafness, autosomal dominant 90		
-MONDO:0958233	bethlem myopathy 1b	OMIM:620725	MONDO:equivalentTo	bethlem myopathy 1b		
-MONDO:0958234	bethlem myopathy 1c	OMIM:620726	MONDO:equivalentTo	bethlem myopathy 1c		
-MONDO:0958235	ullrich congenital muscular dystrophy 1b	OMIM:620727	MONDO:equivalentTo	ullrich congenital muscular dystrophy 1b		
-MONDO:0958236	ullrich congenital muscular dystrophy 1c	OMIM:620728	MONDO:equivalentTo	ullrich congenital muscular dystrophy 1c		
-MONDO:0958237	hyperferritinemia	OMIM:620729	MONDO:equivalentTo	hyperferritinemia		
-MONDO:0958238	hyperemesis gravidarum, susceptibility to	OMIM:620730	MONDO:equivalentTo	hyperemesis gravidarum, susceptibility to		
-MONDO:0958239	microphthalmia/coloboma 11	OMIM:620731	MONDO:equivalentTo	microphthalmia/coloboma 11		
-MONDO:0958240	neurodevelopmental disorder with hyperkinetic movements, seizures, and structural brain abnormalities	OMIM:620732	MONDO:equivalentTo	neurodevelopmental disorder with hyperkinetic movements, seizures, and structural brain abnormalities		
-MONDO:0958241	cardiomyopathy, familial hypertrophic, 30, atrial	OMIM:620734	MONDO:equivalentTo	cardiomyopathy, familial hypertrophic, 30, atrial		
-MONDO:0958242	spermatogenic failure 90	OMIM:620744	MONDO:equivalentTo	spermatogenic failure 90		
-MONDO:0958277	deafness, autosomal recessive 123	OMIM:620745	MONDO:equivalentTo	deafness, autosomal recessive 123		
-MONDO:0958278	neurodevelopmental disorder with hypotonia and characteristic brain abnormalities	OMIM:620746	MONDO:equivalentTo	neurodevelopmental disorder with hypotonia and characteristic brain abnormalities		
-MONDO:0958279	megalencephaly-polydactyly syndrome	OMIM:620748	MONDO:equivalentTo	megalencephaly-polydactyly syndrome		
+MONDO:0958230	orofaciodigital syndrome 20	OMIM:620718	MONDO:equivalentTo	orofaciodigital syndrome 20		MONDO:0015375
+MONDO:0958232	deafness, autosomal dominant 90	OMIM:620722	MONDO:equivalentTo	deafness, autosomal dominant 90		MONDO:0019587
+MONDO:0958281	branchiootorenal syndrome	OMIMPS:113650	MONDO:equivalentTo	Branchiootorenal syndrome		
+MONDO:0958282	palmoplantar keratoderma, epidermolytic	OMIMPS:144200	MONDO:equivalentTo	Palmoplantar keratoderma, epidermolytic		
+MONDO:0958283	li-fraumeni syndrome	OMIMPS:151623	MONDO:equivalentTo	Li-Fraumeni syndrome		
+MONDO:0958284	branchiootic syndrome	OMIMPS:602588	MONDO:equivalentTo	Branchiootic syndrome