Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B901a112d4b98b5a50f66ee20713c74cb> ?p ?o ?g. }
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- B901a112d4b98b5a50f66ee20713c74cb hasDbXref "Orphanet:141209" @default.
- B901a112d4b98b5a50f66ee20713c74cb type Axiom @default.
- B901a112d4b98b5a50f66ee20713c74cb annotatedProperty IAO_0000115 @default.
- B901a112d4b98b5a50f66ee20713c74cb annotatedSource MONDO_0015408 @default.
- B901a112d4b98b5a50f66ee20713c74cb annotatedTarget "A rare developmental defect during embryogenesis characterized by multifocal dilated lymphatic vessels involving multiple organs and tissues. Patients mostly present in infancy and childhood. Clinical course and prognosis depend on the affected sites and extent of the condition, deterioration of lung function being a major cause of morbidity and mortality." @default.