Autosomal recessive secondary polycythemia not associated with VHL gene
Synonyms: Autosomal recessive secondary erythrocytosis not associated with VHL gene | Autosomal recessive secondary erythrocytosis, non-Chuvash type | Autosomal recessive secondary polycythemia, non-Chuvash type
A rare hereditary hematologic disease characterized by an increase in hemoglobin hematocrit and erythrocyte mass resulting in plethora or ruddy complexion headache dizziness tinnitus and exertional dyspnea. In some cases thrombophlebitis and arthralgia have also been reported.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Autosomal recessive secondary polycythemia not associated with VHL gene?
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Advocacy Organizations
Care-for-Rare America Inc
To establish a global alliance in order to identify the genetic causes of rare diseases and develop effective treatments, following a three-stage approach: recognize, understand, cure.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Youth And Women for Opportunities Uganda-YWOU
Our mission supports Rare, orphan and undiagnosed diseases diagnosis, care and treatment, education, awareness and empowering health care professionals and patients care takers of rare, orphan and undiagnosed diseases arena in Uganda, build capacity and bridge lack of clinical knowledge and experience and provide search/quest for diagnostic laboratories, I advocate for changes in laws, practices
Clinical Trials
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