Omodysplasia 1

Alternate names[edit | edit source]

OMOD1; Omodysplasia generalized form; Omodysplasia autosomal recessive; Micromelic dysplasia congenita with dislocation of radius

An autosomal recessive generalised form of omodysplasia, a rare skeletal dysplasia, with characteristics of severe micromelic dwarfism with predominantly rhizomelic shortening of both the upper and lower limbs.

NIH genetic and rare disease info[edit source]

NIH info on Omodysplasia 1

Omodysplasia 1 is a rare disease.

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Rare diseases - Omodysplasia 1
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Also see	Comprehensive list of genetic and rare diseases
Resources	NIH GARD, US Genetic and Rare Diseases Info Rare Disease Day Undiagnosed Diseases Network Database of rare diseases at Orphanet Rare Disease UK Rare diseases search engine