Q85.0 is the ICD-10 code for Neurofibromatosis (nonmalignant). It is a four-character subcategory of Q85 (Phakomatoses, not elsewhere classified), the most specific level in the WHO edition. It belongs to the block Q80–Q89 (Other congenital malformations) in Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities.
- Code type
- Subcategory (4 characters)
- Chapter
- XVII · Q00–Q99
- Classification
- WHO ICD-10, 2019 version
What Q85.0 includes
Conditions and terms that are coded here.
- Von Recklinghausen disease
Q85.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
Q85.0Nevrofibromatose
- Q85.01Nevrofibromatose type 1
- Q85.02Nevrofibromatose type 2
DQ850Ikke-malign neurofibromatose
Q85.0Neurofibromatoosi
- Q85.00Neurofibromatoosi, tyyppi 1
- Q85.01Neurofibromatoosi, tyyppi 2
- Q85.09Määrittämätön neurofibromatoosi
Q85.0Neurofibromatose (nicht bösartig)
Q85.0Neurofibromatose (non maligne)
Q85.0neurofibromatose (niet-maligne)
Listed through more specific codes:
- Q85.00Neurofibromatosis, unspecified
- Q85.01Neurofibromatosis, type 1
- Q85.02Neurofibromatosis, type 2
- Q85.03Schwannomatosis
- Q85.09Other neurofibromatosis
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.
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