3B60.0ICD-11 MMS 2026-01
Hereditary vascular purpura
Index terms
- Hereditary vascular purpura
- Hereditary capillary fragility
Exclusions from above levels
3B64.14– Thrombotic thrombocytopenic purpura4A44.9– Immune complex small vessel vasculitis4A44.A– Antineutrophil cytoplasmic antibody-associated vasculitis
Show allHide
4A44.B– Leukocytoclastic vasculitis4A45– Antiphospholipid syndrome4A85.03– Drug-associated immune complex vasculitisEE40.32– Purpura or bruising due to vascular fragilityEF31– Traumatic purpuraJA43.3– Postpartum coagulation defects04– Diseases of the immune system05– Endocrine, nutritional or metabolic diseases18– Complications of pregnancy, childbirth or the puerperium19– Certain conditions originating in the perinatal period20– Congenital malformations, deformations or chromosomal abnormalities22– Injury, poisoning or certain other consequences of external causes- http://id.who.int/icd/entity/1000704511 – Human immunodeficiency virus disease
JB64.1– Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium
Sibling codes
3B60.1– Acquired vascular purpura
Foundation entity
Hereditary vascular purpura – http://id.who.int/icd/entity/1912288163
Part of: 3B60: Non-thrombocytopenic purpura › 03: Diseases of the blood or blood-forming organs