Achondroplasia and Swiss type agammaglobulinemia

Symptoms of Achondroplasia and Swiss type agammaglobulinemia

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:

Treatments

See also the following treatment articles:

Causes

See also causal information:

Genetics

See also genetics of related diseases:

Similar Topic Articles

Names and Terminology

Other Names: Agammaglobulinemia and achondroplasia ...Source: GARD (NIH)1 ...

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References

  1. Source: GARD (NIH): rarediseases.info.nih.gov/ diseases/ 463/ achondroplasia-and-swiss-type-agammaglobulinemia

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