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Dictionary » Heterozygous OSMED
 

Heterozygous OSMED

Introduction: Heterozygous OSMED

Description of Heterozygous OSMED

Heterozygous OSMED (medical condition): A very rare inherited disorder involving bone growth...more »

See also:

Pierre-Robin syndrome with fetal chondrodysplasia:
  »Introduction: Pierre-Robin syndrome with fetal chondrodysplasia
  »Symptoms of Pierre-Robin syndrome with fetal chondrodysplasia

Heterozygous OSMED: Related Topics

These medical condition or symptom topics may be relevant to medical information for Heterozygous OSMED:

Heterozygous OSMED as a Disease

Heterozygous OSMED: Another name for Pierre-Robin syndrome with fetal chondrodysplasia (or close medical condition association).
  »Introduction: Pierre-Robin syndrome with fetal chondrodysplasia
  »Symptoms of Pierre-Robin syndrome with fetal chondrodysplasia

Heterozygous OSMED: Related Diseases

Heterozygous OSMED: Heterozygous OSMED is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Heterozygous OSMED (Pierre-Robin syndrome with fetal chondrodysplasia)

Some of the symptoms of Heterozygous OSMED incude:

  • Small jaw
  • Rhizomelic chondrodysplasia
  • Dumbbell-shaped thigh bone
  • Dumbbell-shaped upper arm bone
  • Myopia

Heterozygous OSMED: Related Disease Topics

These medical disease topics may be related to Heterozygous OSMED:

  • skeltal abnormalities
  • haering loss
  • otospondlyomegaepiphyseal dysplasia
  • cleft palate
  • wide protruding eyes
  • dumb-bell shaped bones

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