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Dictionary » Familial dyschondroplasia
 

Familial dyschondroplasia

Introduction: Familial dyschondroplasia

Description of Familial dyschondroplasia

Familial dyschondroplasia (medical condition): A rare condition characterized by pelvic anomalies and multiple bone tumors....more »

See also:

Upington disease:
  »Introduction: Upington disease
  »Symptoms of Upington disease

Familial dyschondroplasia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial dyschondroplasia:

Familial dyschondroplasia: Rare Disease

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

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

Familial dyschondroplasia as a Disease

Familial dyschondroplasia: Another name for Upington disease (or close medical condition association).
  »Introduction: Upington disease
  »Symptoms of Upington disease

Familial dyschondroplasia: Related Diseases

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

Symptoms of Familial dyschondroplasia (Upington disease)

Some of the symptoms of Familial dyschondroplasia incude:

  • Coxa vera
  • Pelvis anomaly
  • Absent femur
  • Poor joint mobility
  • Enchondromata

Familial dyschondroplasia: Related Disease Topics

These medical disease topics may be related to Familial dyschondroplasia:

Terms associated with Familial dyschondroplasia:

Terms Similar to Familial dyschondroplasia:

Source - NIH

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Medical dictionaries:

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