287.33 - Congenital And Hereditary Thrombocytopenic Purpura
The ICD 9 Code for Congenital and hereditary thrombocytopenic purpura is listed as 287.33.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | 287.33 |
| Long Description: | Congenital and hereditary thrombocytopenic purpura |
| Short Description: | Cong/herid thromb purpra |
| Chapter: | Diseases Of The Blood And Blood-Forming Organs |
| Block: | Purpura and other hemorrhagic conditions (287-287) |
| Related Descriptions: |
Amegakaryocytic thrombocytopenia with congenital malformation
Congenital thrombocytopenic purpura Hereditary thrombocytopenic disorder Upshaw-Schulman syndrome |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | D69.42 - Congenital and hereditary thrombocytopenia purpura |
| ICD-9-CM Siblings (same level / similar specificity) of 287.33: | |
| 287.30 - Primary thrombocytopenia,unspecified | |
| 287.31 - Immune thrombocytopenic purpura | |
| 287.32 - Evans' syndrome | |
| 287.39 - Other primary thrombocytopenia | |