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Prevalence Statistics for Types of X-linked Dominant Genetic Diseases

Prevalence Statistics for Types of X-linked Dominant Genetic Diseases

The information below shows a list of types of X-linked Dominant Genetic Diseases, with information as to the prevalence of each of these types. Estimates of the people affected are calculated based on the available statistic.

Disease Prevalence Estimate US people estimate Statistic Used for Calculation
Coffin-Lowry syndrome approx 1 in 14,285 or 0.01% or 19,040 people in USA 19,040 estimated 7 per 100,000 people have Coffin-Lowry syndrome in western Europe and North America, Genetics Home Reference website
Incontinentia Pigmenti approx 1 in 388,571 or 0.00% or 700 people in USA 700 700 - 1,000 cases of incontinentia pigmenti have been reported, Genetics Home Reference website
Familial rickets N/A N/A No information
Hereditary nephritis N/A N/A No information

Types of X-linked Dominant Genetic Diseases

For more information about types of X-linked Dominant Genetic Diseases, refer to our section on types of X-linked Dominant Genetic Diseases.

About prevalence:

The medical term 'prevalence' of X-linked Dominant Genetic Diseases usually refers to the estimated population of people who are managing X-linked Dominant Genetic Diseases at any given time, whereas the annual diagnosis rate of new cases of X-linked Dominant Genetic Diseases is called the 'incidence'. For more information on prevalence and incidence statistics, see about prevalence and incidence statistics.

 

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