Autosomal recessive hereditary disorder	Congenital anomaly of limb	Developmental hereditary disorder	Dysostosis	Hereditary disorder of musculoskeletal system	Multiple malformation syndrome with limb defect as major feature
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Fuhrmann syndrome (disorder)
	Fuhrmann syndrome
	Fuhrmann Rieger de Sousa syndrome
	Fuhrmann syndrome is mainly characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly.

Id	721296004
Status	Primitive

Associated morphology	Dysplasia
Finding site	Bone structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Limb structure
Occurrence	Congenital
Pathological process	Pathological developmental process

SNOMED CT to Orphanet simple map

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q74.8
Term	Overige gespecificeerde congenitale misvormingen van extremiteit(en)

SNOMED CT to ICD-10 extended map

Target	Q74.8
Rule	TRUE
Advice	ALWAYS Q74.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified