Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be6a5d6a95e8f31cd85f8bc71c4d9a0b3> ?p ?o ?g. }
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- Be6a5d6a95e8f31cd85f8bc71c4d9a0b3 hasDbXref "GARD:0003995" @default.
- Be6a5d6a95e8f31cd85f8bc71c4d9a0b3 type Axiom @default.
- Be6a5d6a95e8f31cd85f8bc71c4d9a0b3 annotatedProperty IAO_0000115 @default.
- Be6a5d6a95e8f31cd85f8bc71c4d9a0b3 annotatedSource MONDO_0044749 @default.
- Be6a5d6a95e8f31cd85f8bc71c4d9a0b3 annotatedTarget "X-linked congenital stationary night blindness (XLCSNB) is a disorder of the retina. People with this condition typically experience night blindness and other vision problems, including loss of sharpness (reduced visual acuity), severe nearsightedness (myopia), nystagmus,and strabismus. Color vision is typically not affected. These vision problems are usually evident at birth, but tend to be stable (stationary) over time. There aretwo major types of XLCSNB: the complete form and the incomplete form. Bothtypes have very similar signs and symptoms. However, everyone with the complete form has night blindness, while not all people with the incomplete form have night blindness. The types are distinguished by their genetic cause." @default.