fuhrmann syndrome

Preferred Label : fuhrmann syndrome;

MeSH note : Bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies; Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly;

Details

Origin ID

C538189;

UMLS CUI

C1856728;

Automatic exact mappings (from CISMeF team)
- Fuhrmann-Rieger-de Sousa syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [OMIM Phenotype]
- Fuhrmann syndrome [DO Concept]
- Fuhrmann syndrome [Disease (Nov.)]
- Fuhrmann syndrome [ORDO Disease]
- Fuhrmann syndrome (disorder) [SNOMED CT concept]
DO Cross reference
- Fuhrmann syndrome [DO Concept]
MeSH term(s) associated for indexing
- foot deformities, congenital [MeSH Descriptor]
- hand deformities, congenital [MeSH Descriptor]
ORDO relation(s)
- Fuhrmann syndrome [ORDO Disease]
Record concept(s)
- Fuhrmann syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [OMIM Phenotype]
- Fuhrmann syndrome [ORDO Disease]
- Fuhrmann syndrome [DO Concept]
- Fuhrmann syndrome [Disease (Nov.)]
- Fuhrmann syndrome (disorder) [SNOMED CT concept]

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