Primary Raynaud disease

Description

Raynaud phenomenon unassociated with any concomitant disease, drug or other provoking trauma. Criteria for diagnosis include: bilateral symmetrical episodic attacks without evidence of peripheral vascular disease or tissue injury, normal nail fold capillaroscopy, negative antinuclear antibody and normal erythrocyte sedimentation rate.

Index terms

Primary Raynaud disease
Raynaud disease

Inclusions

Raynaud disease

Exclusions from above levels

http://id.who.int/icd/entity/1059873720 – Diseases of coronary artery
01 – Certain infectious or parasitic diseases
05 – Endocrine, nutritional or metabolic diseases

Show allHide

18 – Complications of pregnancy, childbirth and the puerperium
19 – Certain conditions originating in the perinatal period
20 – Congenital malformations, deformations and chromosomal abnormalities
22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

BD42.1 – Secondary Raynaud phenomenon
BD42.Z – Raynaud phenomenon, unspecified

Foundation entity

Primary Raynaud disease – http://id.who.int/icd/entity/1592720372

Part of: BD42: Raynaud phenomenon › 11: Diseases of the circulatory system