Schinzel Giedion Syndrome is a rare genetic disorder characterized by severe intellectual disability, distinctive facial features, skeletal abnormalities, and organ malformations. The ICD-10 code for Schinzel Giedion Syndrome is Q87.1. Unfortunately, there is no specific ICD-9 code for this syndrome as ICD-9 does not provide a direct match for this condition. It is important to consult with a healthcare professional for accurate diagnosis and coding.
Schinzel Giedion Syndrome, also known as Schinzel-Giedion midface retraction syndrome, is an extremely rare genetic disorder. It is characterized by a distinct facial appearance, skeletal abnormalities, and other developmental anomalies. Unfortunately, due to the rarity of this condition, there is no specific ICD10 code assigned solely for Schinzel Giedion Syndrome.
In the International Classification of Diseases, Tenth Revision (ICD10), specific codes are provided for various signs, symptoms, and associated conditions that may be present in individuals with Schinzel Giedion Syndrome. For example, the facial abnormalities can be classified using codes such as Q67.4 (Congenital deformity of skull and face bones) or Q87.0 (Congenital malformation syndromes predominantly affecting facial appearance). Similarly, skeletal abnormalities can be coded using various relevant codes under Q65 (Congenital deformities of the musculoskeletal system).
As for the ICD9 code, the Ninth Revision of the International Classification of Diseases, it is important to note that ICD9 codes were replaced by ICD10 codes on October 1, 2015, in most countries. However, for historical reference, the closest ICD9 codes that may be relevant to Schinzel Giedion Syndrome include 756.0 (Anomalies of skull and face bones) and 756.4 (Anomalies of spine, not elsewhere classified).
It is crucial to consult with a healthcare professional or geneticist for accurate diagnosis, as the ICD codes mentioned above are for reference purposes only and should not be used as a substitute for proper medical evaluation and diagnosis.