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- NCIT_C84835 IAO_0000115 "A rare disorder of unknown etiology. It may present as a cutaneous disorder with a benign clinical course or a systemic disorder with a grim prognosis. Both the cutaneous and systemic variants are characterized by the presence of papular skin lesions. The systemic variant, in addition to the skin papules, is characterized by gastrointestinal manifestations including abdominal pain and distention, nausea, vomiting, diarrhea, intestinal infarction, and intestinal perforation. The central and peripheral nervous systems may also be involved in the systemic variant." @default.
- NCIT_C84835 NCIT_NHC0 "C84835" @default.
- NCIT_C84835 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C84835 NCIT_P108 "Malignant Atrophic Papulosis" @default.
- NCIT_C84835 NCIT_P207 "C0221011" @default.
- NCIT_C84835 normalizedInformationContent "100" @default.
- NCIT_C84835 referenceCount "1" @default.
- NCIT_C84835 hasExactSynonym "Degos Disease" @default.
- NCIT_C84835 hasExactSynonym "Malignant Atrophic Papulosis" @default.
- NCIT_C84835 type Class @default.
- NCIT_C84835 isDefinedBy ncit.owl @default.
- NCIT_C84835 label "Malignant Atrophic Papulosis" @default.
- NCIT_C84835 subClassOf NCIT_C2991 @default.
- NCIT_C84835 subClassOf NCIT_C4873 @default.
- NCIT_C84835 subClassOf NCIT_C53529 @default.
- NCIT_C84835 subClassOf NCIT_C53543 @default.
- NCIT_C84835 subClassOf NCIT_C53547 @default.
- NCIT_C84835 subClassOf NCIT_C7057 @default.
- NCIT_C84835 subClassOf NCIT_C84835 @default.