Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bbf8c910ec26f6be2e43e642aecfa1dfd> ?p ?o ?g. }
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- Bbf8c910ec26f6be2e43e642aecfa1dfd hasDbXref "Orphanet:2526" @default.
- Bbf8c910ec26f6be2e43e642aecfa1dfd type Axiom @default.
- Bbf8c910ec26f6be2e43e642aecfa1dfd annotatedProperty IAO_0000115 @default.
- Bbf8c910ec26f6be2e43e642aecfa1dfd annotatedSource MONDO_0007918 @default.
- Bbf8c910ec26f6be2e43e642aecfa1dfd 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.