Q95.5 is the ICD-10 code for Individuals with autosomal fragile site. It is a four-character subcategory of Q95 (Balanced rearrangements and structural markers, not elsewhere classified), the most specific level in the WHO edition. It belongs to the block Q90–Q99 (Chromosomal abnormalities, not elsewhere classified) in Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities.
- Code type
- Subcategory (4 characters)
- Chapter
- XVII · Q00–Q99
- Classification
- WHO ICD-10, 2019 version
Q95.5 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
Q95.5Individer med autosomalt fragilt sted
DQ955Autosomalt kromosom med fragilt sted
Q95.5Autosomin säröalue (frax, fragile site)
Q95.5Individuen mit autosomaler Bruchstelle
Q95.5Sujet avec site autosomique fragile
Q95.5individuen met breekbare plaats op autosoom
Q95.5Individual with autosomal fragile site
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
Look up another code
Stop looking codes up by hand
Docdemic listens to the consultation, writes the note and suggests the diagnosis and procedure codes that fit it, each one checked against your country’s official code list.
Try Docdemic free