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- NCIT_C156032 IAO_0000115 "A group of inherited skin disorders that present with multisystem involvement. It includes ichthyosis, epidermolysis bullosa, ectodermal dysplasia, cutis laxa, progeroid conditions, xeroderma pigmentosum, Rothmund Thomson syndrome, and dyskeratosis congenita." @default.
- NCIT_C156032 NCIT_NHC0 "C156032" @default.
- NCIT_C156032 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C156032 NCIT_P107 "Genodermatosis" @default.
- NCIT_C156032 NCIT_P108 "Genodermatosis" @default.
- NCIT_C156032 NCIT_P207 "C0037277" @default.
- NCIT_C156032 NCIT_P322 "CTRP" @default.
- NCIT_C156032 NCIT_R100 NCIT_C12219 @default.
- NCIT_C156032 NCIT_R100 NCIT_C12907 @default.
- NCIT_C156032 NCIT_R100 NCIT_C12919 @default.
- NCIT_C156032 NCIT_R108 NCIT_C3367 @default.
- NCIT_C156032 NCIT_R108 NCIT_C36278 @default.
- NCIT_C156032 NCIT_R108 NCIT_C36281 @default.
- NCIT_C156032 NCIT_R108 NCIT_C39570 @default.
- NCIT_C156032 NCIT_R108 NCIT_C7057 @default.
- NCIT_C156032 normalizedInformationContent "71.700606907059111" @default.
- NCIT_C156032 referenceCount "72" @default.
- NCIT_C156032 hasExactSynonym "Genodermatosis" @default.
- NCIT_C156032 inSubset NCIT_C116977 @default.
- NCIT_C156032 inSubset NCIT_C118168 @default.
- NCIT_C156032 type Class @default.
- NCIT_C156032 isDefinedBy ncit.owl @default.
- NCIT_C156032 label "Genodermatosis" @default.
- NCIT_C156032 subClassOf NCIT_C156032 @default.
- NCIT_C156032 subClassOf NCIT_C27551 @default.
- NCIT_C156032 subClassOf NCIT_C2849 @default.
- NCIT_C156032 subClassOf NCIT_C2991 @default.
- NCIT_C156032 subClassOf NCIT_C3371 @default.
- NCIT_C156032 subClassOf NCIT_C36287 @default.
- NCIT_C156032 subClassOf NCIT_C53529 @default.
- NCIT_C156032 subClassOf NCIT_C53547 @default.
- NCIT_C156032 subClassOf NCIT_C7057 @default.
- NCIT_C156032 subClassOf NCIT_C97151 @default.
- NCIT_C156032 subClassOf NCIT_C97174 @default.