ICD-9 Diagnosis Code 758.81

Oth cond due to sex chrm

Diagnosis Code 758.81

ICD-9: 758.81
Short Description: Oth cond due to sex chrm
Long Description: Other conditions due to sex chromosome anomalies
This is the 2014 version of the ICD-9-CM diagnosis code 758.81

Code Classification
  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 758 Chromosomal anomalies

Information for Medical Professionals

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The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • 18p partial monosomy syndrome
  • 46, XX true hermaphrodite
  • Absence of sex chromosome
  • Additional sex chromosome
  • Anomaly of chromosome X
  • Anomaly of chromosome Y
  • Anomaly of sex chromosome
  • Barr body absent, nuclear sex male
  • Barr body, more than one present per cell
  • Chimera 46, XX; 46, XY
  • Double Y syndrome
  • Female with more than three X chromosomes
  • Four X syndrome
  • Fragile X chromosome
  • Karyotype 46, X iso
  • Karyotype 46, X with abnormal sex chromosome except iso
  • Male with structurally abnormal sex chromosome
  • Mosaic including XXXXY
  • Mosaic XO/XX
  • Mosaic XO/XY
  • Mosaic XY/XXY
  • Mosaicism - lines with various numbers of X chromosomes
  • Mosaicism 45, X / other cell line with abnormal sex chromosome
  • Penta X syndrome
  • Sex chromosome abnormality - female phenotype
  • Sex chromosome abnormality - male phenotype
  • Sex chromosome mosaicism
  • Sex phenotype-karyotype dissociation syndrome
  • Sex-linked hereditary disorder
  • Tetrasomy 12p
  • Triple X syndrome, epilepsy, and hypogammaglobulinemia
  • Trisomy X syndrome
  • Virilization of female due to SOX9 gene duplication
  • Virilization of female due to SRY gene translocation
  • X-linked creatine deficiency
  • X-linked intellectual deficit-dystonia-dysarthria syndrome
  • XX males
  • XXXXY syndrome
  • XXXY syndrome
  • XXYY syndrome
  • XY females
  • XY, female phenotype

Index of Diseases and Injuries
References found for the code 758.81 in the Index of Diseases and Injuries:

Information for Patients

Genetic Disorders

Genes are the building blocks of heredity. They are passed from parent to child. They hold DNA, the instructions for making proteins. Proteins do most of the work in cells. They move molecules from one place to another, build structures, break down toxins, and do many other maintenance jobs.

Sometimes there is a mutation, a change in a gene or genes. The mutation changes the gene's instructions for making a protein, so the protein does not work properly or is missing entirely. This can cause a medical condition called a genetic disorder.

You can inherit a gene mutation from one or both parents. A mutation can also happen during your lifetime.

There are three types of genetic disorders:

  • Single-gene disorders, where a mutation affects one gene. Sickle cell anemia is an example.
  • Chromosomal disorders, where chromosomes (or parts of chromosomes) are missing or changed. Chromosomes are the structures that hold our genes. Down syndrome is a chromosomal disorder.
  • Complex disorders, where there are mutations in two or more genes. Often your lifestyle and environment also play a role. Colon cancer is an example.

Genetic tests on blood and other tissue can identify genetic disorders.

NIH: National Library of Medicine

  • Genetics

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