jacobs syndrome

Preferred Label : jacobs syndrome;

MeSH synonym : congenital familial hypertrophic synovitis; fibrosing serositis, familial; arthropathy camptodactyly syndrome; camptodactyly-arthropathy-coxa vara-pericarditis syndrome; camptodactyly arthropathy pericarditis syndrome; pericarditis arthropathy camptodactyly syndrome; hypertrophic synovitis, congenital familial; Pericarditis-Arthropathy-Camptodactyly syndrome; Arthropathy-Camptodactyly syndrome; Camptodactyly-Arthropathy-Pericarditis syndrome;

Details

Origin ID

C537560;

UMLS CUI

C1859690;

Automatic exact mappings (from CISMeF team)
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) [SNOMED CT concept]
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome [OMIM Phenotype]
- Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome [ORDO Disease]
- camptodactyly-arthropathy-coxa vara-pericarditis syndrome [DO Concept]
DO Cross reference
- camptodactyly-arthropathy-coxa vara-pericarditis syndrome [DO Concept]
MeSH term(s) associated for indexing
- arthropathy, neurogenic [MeSH Descriptor]
- coxa vara [MeSH Descriptor]
- hand deformities, congenital [MeSH Descriptor]
- synovitis [MeSH Descriptor]
Record concept(s)
- Jacobs syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) [SNOMED CT concept]
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome [OMIM Phenotype]
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome [MedDRA Preferred Term]
- Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome [ORDO Disease]
- camptodactyly-arthropathy-coxa vara-pericarditis syndrome [DO Concept]

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