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ICD-10-CM Code D69.42
Congenital and hereditary thrombocytopenia purpura

BILLABLE
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

D69.42 is a billable ICD code used to specify a diagnosis of congenital and hereditary thrombocytopenia purpura. A 'billable code' is detailed enough to be used to specify a medical diagnosis.


The ICD code D69 is used to code Purpura

Purpura is a condition of red or purple discolored spots on the skin that do not blanch on applying pressure. The spots are caused by bleeding underneath the skin usually secondary to vasculitis or dietary deficiency of vitamin C (scurvy). They measure 0.3–1 cm (3–10 mm), whereas petechiae measure less than 3 mm, and ecchymoses greater than 1 cm.

Specialty: Dermatology, Hematology
MeSH Code: D011693
ICD 9 Code: 287

Petechiae and purpura on the lower limb due to medication induced vasculitis

Source: Wikipedia

Coding Notes for D69.42 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Congenital thrombocytopenia
Hereditary thrombocytopenia
codeFirst:
Congential or hereditary disorder, such as:
Thrombocytopenia with absent radius (TAR syndrome) See code Q87.2

MS-DRG Mapping

  • DRG Group #813 - Coagulation disorders.

Related Concepts SNOMET-CT

  • Amegakaryocytic thrombocytopenia with congenital malformation (disorder)

Coding Advice SNOMET-CT

  • Consider additional code to identify specific condition or disease

ICD-10-CM Alphabetical Index References for 'D69.42 - Congenital and hereditary thrombocytopenia purpura'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D69.42. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

Congenital and hereditary thrombocytopenic purpura (exact match)

This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 287.33 was previously used, D69.42 is the appropriate modern ICD10 code.


Parent Code: D69.4 - Other primary thrombocytopenia

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/D6942