ICD10 code of Roberts Syndrome and ICD9 code

Roberts Syndrome, also known as Roberts-SC phocomelia syndrome, is a rare genetic disorder characterized by limb and facial abnormalities. It is classified under the International Classification of Diseases, Tenth Revision (ICD-10) and the International Classification of Diseases, Ninth Revision (ICD-9) coding systems. Let's explore the ICD-10 and ICD-9 codes for Roberts Syndrome.

ICD-10 Code for Roberts Syndrome:

In the ICD-10 coding system, Roberts Syndrome is classified under the Q87.1 code. The Q87 category represents "Other specified congenital malformation syndromes affecting multiple systems." Within this category, Q87.1 specifically refers to "Congenital malformation syndromes predominantly affecting facial appearance." Roberts Syndrome falls under this classification due to its characteristic facial abnormalities.

The ICD-10 code for Roberts Syndrome is Q87.1.

ICD-9 Code for Roberts Syndrome:

In the ICD-9 coding system, Roberts Syndrome is classified under the 756.89 code. The 756 category represents "Other congenital musculoskeletal anomalies." Within this category, 756.89 specifically refers to "Other specified congenital musculoskeletal anomalies." Roberts Syndrome is included in this classification due to its limb abnormalities.

The ICD-9 code for Roberts Syndrome is 756.89.

Summary:

Roberts Syndrome is a rare genetic disorder characterized by limb and facial abnormalities. In the ICD-10 coding system, it is classified under the Q87.1 code, which represents congenital malformation syndromes predominantly affecting facial appearance. In the ICD-9 coding system, it is classified under the 756.89 code, which represents other specified congenital musculoskeletal anomalies.