Autosomal dominant hereditary disorder	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Mesomelic dysplasia
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Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder)
	Reinhardt Pfeiffer mesomelic dysplasia
	Mesomelic dwarfism Reinhardt-Pfeiffer type Reinhardt Pfeiffer syndrome Mesomelic dysplasia of hypoplastic ulna and fibula type
	Disproportionate short stature present from birth with dysplasia of the ulna and fibula. Curvatures of the forearm, radial head luxation, and tibial anomalies have also been described. The syndrome is transmitted in an autosomal dominant manner.
	mesomele dwerggroei Reinhardt-Pfeiffer-type
	mesomele dysplasie type Reinhardt-Pfeiffer syndroom van Reinhardt-Pfeiffer

Id	715472000
Status	Primitive

Associated morphology	Dysplasia
Finding site	Skeletal system structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Clinical course

Interprets

Height / growth measure

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q78.8
Rule	TRUE
Advice	ALWAYS Q78.8
Correlation	SNOMED CT source code to target map code correlation not specified