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- NCIT_C125383 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the SCN9A gene, encoding sodium channel protein type 9 subunit alpha. It is characterized by episodes of recurrent warmth, redness, and burning sensations in the extremities." @default.
- NCIT_C125383 NCIT_NHC0 "C125383" @default.
- NCIT_C125383 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C125383 NCIT_P108 "Primary Erythromelalgia" @default.
- NCIT_C125383 NCIT_P207 "C0014805" @default.
- NCIT_C125383 NCIT_P322 "Cellosaurus" @default.
- NCIT_C125383 NCIT_R176 NCIT_C114810 @default.
- NCIT_C125383 NCIT_R176 NCIT_C16612 @default.
- NCIT_C125383 NCIT_R176 NCIT_C21295 @default.
- NCIT_C125383 NCIT_R176 NCIT_C25869 @default.
- NCIT_C125383 NCIT_R176 NCIT_C25993 @default.
- NCIT_C125383 NCIT_R176 NCIT_C26039 @default.
- NCIT_C125383 NCIT_R176 NCIT_C28533 @default.
- NCIT_C125383 normalizedInformationContent "100" @default.
- NCIT_C125383 referenceCount "1" @default.
- NCIT_C125383 hasExactSynonym "PERYTHM" @default.
- NCIT_C125383 hasExactSynonym "Primary Erythermalgia" @default.
- NCIT_C125383 hasExactSynonym "Primary Erythromelalgia" @default.
- NCIT_C125383 inSubset NCIT_C165258 @default.
- NCIT_C125383 inSubset NCIT_C192842 @default.
- NCIT_C125383 type Class @default.
- NCIT_C125383 isDefinedBy ncit.owl @default.
- NCIT_C125383 label "Primary Erythromelalgia" @default.
- NCIT_C125383 subClassOf Bb35cbc5f61a6403ba696cbbbca790162 @default.
- NCIT_C125383 subClassOf Bd924474fc577727390fbf0c22110d8c6 @default.
- NCIT_C125383 subClassOf NCIT_C125383 @default.
- NCIT_C125383 subClassOf NCIT_C2991 @default.
- NCIT_C125383 subClassOf NCIT_C34593 @default.
- NCIT_C125383 subClassOf NCIT_C4873 @default.
- NCIT_C125383 subClassOf NCIT_C53529 @default.
- NCIT_C125383 subClassOf NCIT_C53543 @default.
- NCIT_C125383 subClassOf NCIT_C53547 @default.
- NCIT_C125383 subClassOf NCIT_C7057 @default.