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Dictionary » OSMED Syndrome
 

OSMED Syndrome

Introduction: OSMED Syndrome

Description of OSMED Syndrome

OSMED Syndrome (medical condition): A rare genetic disorder where abnormal bone growth...more »

See also:

Otospondylomegaepiphyseal dysplasia:
  »Introduction: Otospondylomegaepiphyseal dysplasia
  »Symptoms of Otospondylomegaepiphyseal dysplasia
  »Causes of Otospondylomegaepiphyseal dysplasia

OSMED Syndrome: Related Topics

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

OSMED Syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

OSMED Syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that OSMED Syndrome, or a subtype of OSMED Syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

OSMED Syndrome as a Disease

OSMED Syndrome: Another name for Otospondylomegaepiphyseal dysplasia (or close medical condition association).
  »Introduction: Otospondylomegaepiphyseal dysplasia
  »Symptoms of Otospondylomegaepiphyseal dysplasia
  »Causes of Otospondylomegaepiphyseal dysplasia

OSMED Syndrome: Related Diseases

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

Causes of OSMED Syndrome

Some of the causes of OSMED Syndrome are included in the list below:

  • The genetic condition is inherited in an autosomal recessive manner

Symptoms of OSMED Syndrome (Otospondylomegaepiphyseal dysplasia)

Some of the symptoms of OSMED Syndrome incude:

OSMED Syndrome: Related Disease Topics

These medical disease topics may be related to OSMED Syndrome:

Terms associated with OSMED Syndrome:

Terms Similar to OSMED Syndrome:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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