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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Alveolar capillary dysplasia

Other Names for this Disease
  • Congenital alveolar capillary dysplasia
  • Familial persistent pulmonary hypertension of the newborn
  • Pulmonary hypertension, familial persistent of the newborn
More Names
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Overview


These Web pages are updated as the Genetic and Rare Diseases Information Center receives questions and as new information becomes available. If you don’t see many information resources on this page, it may be because the Information Center hasn’t yet received a question about this condition.

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by the Genetic and Rare Diseases Information Center

Please contact us with your questions about Alveolar capillary dysplasia. We will answer your question and update these pages with new resources and information.
On this page

General Information

  • Genetics Home Reference (GHR) contains information on Alveolar capillary dysplasia. Click on the link to go to GHR and review the information.
  • The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs.  Access to this database is free of charge.  Click on the link to read information on this topic.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Alveolar capillary dysplasia. Click on the link to view a sample search on this topic.
  • The The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Alveolar capillary dysplasia. Click on the link to go to OMIM and review these resources.