Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bdfcfa04c921cb67ea8dbdf4153804ad3> ?p ?o ?g. }
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- Bdfcfa04c921cb67ea8dbdf4153804ad3 hasDbXref "Orphanet:49382" @default.
- Bdfcfa04c921cb67ea8dbdf4153804ad3 type Axiom @default.
- Bdfcfa04c921cb67ea8dbdf4153804ad3 annotatedProperty IAO_0000115 @default.
- Bdfcfa04c921cb67ea8dbdf4153804ad3 annotatedSource MONDO_0018852 @default.
- Bdfcfa04c921cb67ea8dbdf4153804ad3 annotatedTarget "Achromatopsia (ACHM) is a rare autosomal recessive retinal disorder characterized by color blindness, nystagmus, photophobia, and severely reduced visual acuity due to the absence or impairment of cone function." @default.