3B64.00ICD-11 MMS 2026-01
Congenital non-inherited thrombocytopenia
Index terms
- Congenital non-inherited thrombocytopenia
- Fetal or neonatal alloimmune thrombocytopenia
- FNAIT - [fetal or neonatal alloimmune thrombocytopenia]
Show allHide
- NAIT - [neonatal alloimmune thrombocytopenia]
- fetal or neonatal thrombocytopenia due to maternal idiopathic thrombocytopenic purpura
- Fetal and neonatal thrombocytopenia due to maternal ITP - [idiopathic thrombocytopenic purpura]
- Neonatal thrombocytopenia due to maternal idiopathic thrombocytopenic purpura
Exclusions from above levels
JA43.3– Postpartum coagulation defects04– Diseases of the immune system05– Endocrine, nutritional or metabolic diseases
Show allHide
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
Foundation children elsewhere
KA89– Transient neonatal thrombocytopaenia
Sibling codes
Foundation entity
Congenital non-inherited thrombocytopenia – http://id.who.int/icd/entity/1374965372
Part of: 3B64.0: Congenital thrombocytopenia › 3B64: Thrombocytopenia › 03: Diseases of the blood or blood-forming organs