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- B2a0de25c1068b07e806db8f3a9be5d9c hasDbXref "NCIT:C72070" @default.
- B2a0de25c1068b07e806db8f3a9be5d9c type Axiom @default.
- B2a0de25c1068b07e806db8f3a9be5d9c annotatedProperty IAO_0000115 @default.
- B2a0de25c1068b07e806db8f3a9be5d9c annotatedSource MONDO_0005100 @default.
- B2a0de25c1068b07e806db8f3a9be5d9c annotatedTarget "A chronic disorder, possibly autoimmune, marked by excessive production of collagen which results in hardening and thickening of body tissues. The two types of systemic scleroderma, limited cutaneous and diffuse cutaneous are classified with focus on the extent of affected skin. A relationship exists between the extent of skin area affected and degree of internal organ/system involvement. Systemic scleroderma can manifest itself in pulmonary fibrosis, Raynaud's syndrome, digestive system telangiectasias, renal hypertension and/or pulmonary hypertension." @default.