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ACG1A

Introduction: ACG1A

Description of ACG1A

ACG1A (medical condition): A rare genetic disorder characterized by abnormal cartilage formation and...more »

See also:

Achondrogenesis type 1A:
  »Introduction: Achondrogenesis type 1A
  »Symptoms of Achondrogenesis type 1A

ACG1A: Rare Disease

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

ACG1A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ACG1A, or a subtype of ACG1A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

ACG1A as a Disease

ACG1A: Another name for Achondrogenesis type 1A (or close medical condition association).
  »Introduction: Achondrogenesis type 1A
  »Symptoms of Achondrogenesis type 1A

ACG1A: Related Diseases

ACG1A: ACG1A is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of ACG1A (Achondrogenesis type 1A)

Some of the symptoms of ACG1A incude:

Terms associated with ACG1A:

Terms Similar to ACG1A:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Ossification anomalies -- psychomotor development delay
  • Ossification center
  • Ossification of Posterior Longitudinal Ligament
  • Ossification of posterior longitudinal ligament in cervical region
  • Ossification of the posterior longitudinal ligament of the spine
  • Ossification, Heterotopic
  • Ossiform
  • Ossify
  • Ossifying cartilage
  • OST
  • Osteal

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