Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B7afda711ee518e2e9a8158c3a21dbfb8> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B7afda711ee518e2e9a8158c3a21dbfb8 hasDbXref "Orphanet:85332" @default.
- B7afda711ee518e2e9a8158c3a21dbfb8 type Axiom @default.
- B7afda711ee518e2e9a8158c3a21dbfb8 annotatedProperty IAO_0000115 @default.
- B7afda711ee518e2e9a8158c3a21dbfb8 annotatedSource MONDO_0010364 @default.
- B7afda711ee518e2e9a8158c3a21dbfb8 annotatedTarget "X-linked intellectual disability-retinitis pigmentosa syndrome is characterized by moderate intellectual deficit and severe, early-onset retinitis pigmentosa. It has been described in five males spanning three generations of one family. Some patients also had microcephaly. It is transmitted as an X-linked recessive trait." @default.