Mesomelic dwarfism, Reinhardt-Pfeiffer type

Preferred Label : Mesomelic dwarfism, Reinhardt-Pfeiffer type;

ICD-11 definition : Mesomelic dwarfism, Reinhardt-Pfeiffer type is a genetic skeletal disordercharacterized by disproportionate short stature from birth with dysplasia of the ulna and fibula.;

Details

Origin ID

1393171517;

Automatic exact mappings (from CISMeF team)
- Mesomelic dwarfism Reinhardt Pfeiffer type [MeSH concept]
- Mesomelic dwarfism, Reinhardt-Pfeiffer type [ORDO Disease]
- Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder) [SNOMED CT concept]
- Ulna and fibula, hypoplasia of [OMIM Phenotype]
- mesomelic dwarfism reinhardt pfeiffer type [MeSH Supplementary Concept]

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