Raynaud Disease

Alias:
Raynaud Phenomenon
Raynaud's Disease
Raynaud's Syndrome
Raynaud's
Secondary Raynaud's Phenomenon
Raynaud's Disease/phenomenon
Cold Fingers, Hereditary
Raynaud's Phenomenon
Raynauds Phenomenon
Raynauds Syndrome
Raynaud Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Raynaud Disease, also known as raynaud phenomenon, is related to antisynthetase syndrome and scleroderma, familial progressive, and has symptoms including abdominal pain, angina pectoris and chest pain. An important gene associated with Raynaud Disease is CENPB (Centromere Protein B), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Diseases of hemostasis. The drugs Cilostazol and Ethanol have been mentioned in the context of this disorder. Affiliated tissues include skin and heart, and related phenotypes are abnormality of the skeletal system and raynaud phenomenon
Related ID:
MESH:D011928
ICD11:1592720372

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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4

Medical Symptom

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Description
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Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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