Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B61958ad6e3019f5455f15e5ecd074c54> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B61958ad6e3019f5455f15e5ecd074c54 hasDbXref "Orphanet:2473" @default.
- B61958ad6e3019f5455f15e5ecd074c54 type Axiom @default.
- B61958ad6e3019f5455f15e5ecd074c54 annotatedProperty IAO_0000115 @default.
- B61958ad6e3019f5455f15e5ecd074c54 annotatedSource MONDO_0009367 @default.
- B61958ad6e3019f5455f15e5ecd074c54 annotatedTarget "McKusick-Kaufman syndrome is a very rare, genetic developmental disorder presenting in the neonatal period characterized by genitourinary malformations, polydactyly, and more rarely, congenital heart disease or gastrointestinal malformations." @default.