Achondrogenesis type 1B

Summary: Achondrogenesis is a group of severe disorders that are present from birth and affect the development of cartilage and bone. Infants with achondrogenesis usually have a small body, short arms and legs, and other skeletal abnormalities that cause life ...1

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Symptoms of Achondrogenesis type 1B

Symptoms: The Human Phenotype Ontology (HPO) provides the following list of features that have been reported in people with this condition. Much of the information in the HPO comes from Orphanet, a European rare disease database. Signs and Symptoms

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Diagnosis

See also related information on diagnosis:

Causes

See also causal information:

Genetics

See also genetics of related diseases:

Names and Terminology

Related Diseases: The following diseases are related to Achondrogenesis type 1B. If you have a question about any of these diseases, you can contact GARD ...2

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References

  1. Source: GARD (NIH): rarediseases.info.nih.gov/ diseases/ 460/ achondrogenesis-type-1b
  2. ibid.

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