Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bdd03cc480ffccb8e9f46e5f40a1fe86d> ?p ?o ?g. }
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- Bdd03cc480ffccb8e9f46e5f40a1fe86d hasDbXref "Orphanet:324" @default.
- Bdd03cc480ffccb8e9f46e5f40a1fe86d type Axiom @default.
- Bdd03cc480ffccb8e9f46e5f40a1fe86d annotatedProperty IAO_0000115 @default.
- Bdd03cc480ffccb8e9f46e5f40a1fe86d annotatedSource MONDO_0010526 @default.
- Bdd03cc480ffccb8e9f46e5f40a1fe86d annotatedTarget "Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations." @default.