mondo_id | mondo_label | xref | xref_source | original_label | definition | parents | subset |
---|---|---|---|---|---|---|---|
ID | LABEL | A oboInOwl:hasDbXref | >A oboInOwl:source SPLIT= | A IAO:0000115 | SC % | ||
MONDO:0971055 | rare yersiniosis | Orphanet:659712 | MONDO:equivalentTo | Rare yersiniosis | MONDO:8000033 | MONDO:0015575 | |
MONDO:0971082 | gastric duplication | Orphanet:662376 | MONDO:equivalentTo | Gastric duplication | MONDO:8000034 | MONDO:8000030 | |
MONDO:0971083 | gallbladder duplication | Orphanet:662388 | MONDO:equivalentTo | Gallbladder duplication | MONDO:0015213 | MONDO:0015116 | |
MONDO:0971084 | colonic duplication | Orphanet:662392 | MONDO:equivalentTo | Colonic duplication | MONDO:0015211 | MONDO:8000030 | |
MONDO:0971085 | pyloric duplication | Orphanet:662405 | MONDO:equivalentTo | Pyloric duplication | MONDO:8000034 | MONDO:8000030 | |
MONDO:0971086 | small intestine duplication | Orphanet:662456 | MONDO:equivalentTo | Small intestine duplication | MONDO:8000030 | MONDO:0015211 | |
MONDO:0971089 | vasa previa | Orphanet:662786 | MONDO:equivalentTo | Vasa previa | MONDO:0015582 | MONDO:8000034 | |
MONDO:0971099 | inherited cancer-predisposing lymphoproliferative syndrome | Orphanet:664450 | MONDO:equivalentTo | Inherited cancer-predisposing lymphoproliferative syndrome | MONDO:8000033 | MONDO:0015356 | |
MONDO:0971100 | immune dysregulation disease with immunodeficiency associated with ebv susceptibility | Orphanet:664456 | MONDO:equivalentTo | Immune dysregulation disease with immunodeficiency associated with EBV susceptibility | MONDO:8000033 | MONDO:0015710 | |
MONDO:0971109 | isolated congenital femoral bifurcation | Orphanet:667589 | MONDO:equivalentTo | Isolated congenital femoral bifurcation | MONDO:8000034 | MONDO:8000030 | |
MONDO:0971120 | syndrome with congenital phagocyte functional defect as a major feature | Orphanet:674648 | MONDO:equivalentTo | Syndrome with congenital phagocyte functional defect as a major feature | MONDO:8000033 | MONDO:0015978 | |
MONDO:0971122 | non-syndromic congenital phagocyte functional defect | Orphanet:674896 | MONDO:equivalentTo | Non-syndromic congenital phagocyte functional defect | MONDO:8000033 | MONDO:0015978 | |
MONDO:0971144 | primary benign peritoneal tumor | Orphanet:676030 | MONDO:equivalentTo | Primary benign peritoneal tumor | MONDO:8000033 | MONDO:0015682 |