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- NCIT_C116916 IAO_0000115 "A rare disorder of unknown etiology, which is characterized by slowly progressive, unilateral facial atrophy of the skin, soft tissue, muscles, and underlying bony structures. Neurological, ocular, and oral symptoms are also often seen, including migraines, trigeminal neuralgia, enophthalmos, and dental and gingival abnormalities." @default.
- NCIT_C116916 NCIT_NHC0 "C116916" @default.
- NCIT_C116916 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C116916 NCIT_P108 "Progressive Hemifacial Atrophy" @default.
- NCIT_C116916 NCIT_P207 "C0015458" @default.
- NCIT_C116916 NCIT_P322 "NICHD" @default.
- NCIT_C116916 NCIT_P325 "A rare disorder characterized by slowly progressive, unilateral facial atrophy of the skin, soft tissue, muscles, and underlying bony structures." @default.
- NCIT_C116916 normalizedInformationContent "100" @default.
- NCIT_C116916 referenceCount "1" @default.
- NCIT_C116916 hasExactSynonym "Parry-Romberg Syndrome" @default.
- NCIT_C116916 hasExactSynonym "Progressive Hemifacial Atrophy" @default.
- NCIT_C116916 inSubset NCIT_C118468 @default.
- NCIT_C116916 inSubset NCIT_C90259 @default.
- NCIT_C116916 type Class @default.
- NCIT_C116916 isDefinedBy ncit.owl @default.
- NCIT_C116916 label "Progressive Hemifacial Atrophy" @default.
- NCIT_C116916 subClassOf NCIT_C116916 @default.
- NCIT_C116916 subClassOf NCIT_C28193 @default.
- NCIT_C116916 subClassOf NCIT_C2991 @default.
- NCIT_C116916 subClassOf NCIT_C7057 @default.