3B11.ZICD-11 MMS 2026-01
Hereditary factor IX deficiency, unspecified
Exclusions from above levels
JA43.3– Postpartum coagulation defects04– Diseases of the immune system05– Endocrine, nutritional or metabolic diseases
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18– 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
Foundation entity
Hereditary factor IX deficiency – http://id.who.int/icd/entity/755266992
Part of: 3B11: Hereditary factor IX deficiency › 03: Diseases of the blood or blood-forming organs