Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3b43df90f43f3830512142d3e4c16699> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B3b43df90f43f3830512142d3e4c16699 hasDbXref "Orphanet:2526" @default.
- B3b43df90f43f3830512142d3e4c16699 type Axiom @default.
- B3b43df90f43f3830512142d3e4c16699 annotatedProperty IAO_0000115 @default.
- B3b43df90f43f3830512142d3e4c16699 annotatedSource MONDO_0007918 @default.
- B3b43df90f43f3830512142d3e4c16699 annotatedTarget "Microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) is a rare autosomal dominant condition characterized by variable expression of microcephaly, ocular disorders including chorioretinopathy, congenital lymphedema of the lower limbs, and mild to moderate intellectual disability." @default.