Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3a01282ea7b0ea90da5c0d9eae818d0d> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B3a01282ea7b0ea90da5c0d9eae818d0d hasDbXref "Orphanet:2786" @default.
- B3a01282ea7b0ea90da5c0d9eae818d0d type Axiom @default.
- B3a01282ea7b0ea90da5c0d9eae818d0d annotatedProperty IAO_0000115 @default.
- B3a01282ea7b0ea90da5c0d9eae818d0d annotatedSource MONDO_0011020 @default.
- B3a01282ea7b0ea90da5c0d9eae818d0d annotatedTarget "Osteoporosis-oculocutaneous hypopigmentation syndrome is characterized by osteoporosis and congenital oculocutaneous hypopigmentation. Three cases have been described in the literature. The mode of inheritance appears to be autosomal recessive." @default.