759.83 FRAGILE X SYNDROME

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Code Information

Diagnosis Code: 759.83

Short Description: Fragile x syndrome

Long Description: Fragile X syndrome

Code Classification:

Congenital anomalies (740–759)
- Congenital anomalies (740-759)
  - 759 Other and unspecified congenital anomalies
    - 759.83 Fragile x syndrome

Code Version: 2015 ICD-9-CM

References to Index of Diseases and Injuries

The code 759.83 has the following ICD-9-CM references to the Index of Diseases and Injuries

Fragile X syndrome 759.83

Syndrome - see also Disease
- fragile X 759.83

Crosswalk Information

The code 759.83 converts into the following ICD-10 code(s):

ICD-9 Code		ICD-10 Code	ICD-10 Description
759.83		Q99.2	Fragile X chromosome

This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code	ICD-9 Description
759.0	Anomalies of spleen
759.1	Anomalies of adrenal gland
759.2	Anomalies of other endocrine glands
759.3	Situs inversus
759.4	Conjoined twins
759.5	Tuberous sclerosis
759.6	Other hamartoses, not elsewhere classified
759.7	Multiple congenital anomalies, so described
759.81	Prader-Willi syndrome
759.82	Marfan syndrome
759.89	Other specified congenital anomalies
759.9	Congenital anomaly, unspecified

This page was last updated on: 10/1/2014

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