Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B2c762213c07243d7a47ca6f75f43fdb0> ?p ?o ?g. }
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- B2c762213c07243d7a47ca6f75f43fdb0 hasDbXref "Orphanet:158025" @default.
- B2c762213c07243d7a47ca6f75f43fdb0 type Axiom @default.
- B2c762213c07243d7a47ca6f75f43fdb0 annotatedProperty IAO_0000115 @default.
- B2c762213c07243d7a47ca6f75f43fdb0 annotatedSource MONDO_0007725 @default.
- B2c762213c07243d7a47ca6f75f43fdb0 annotatedTarget "Hereditary progressive mucinous histiocytosis is a rare, benign, non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, without associated mucosal or visceral involvement. Histologically, papules are well-circumscribed, unencapsulated, nodular aggregates of histiocytes with abundant mucin in the upper and middermis." @default.