| ICD-10-CM-2023 > Q00-Q99 > Q80-Q89 > Q85 |
Q80-Q89 | Other congenital malformations | |
Q85 | Phakomatoses, not elsewhere classified | |
Excl1.: | ataxia telangiectasia [Louis-Bar] (G11.3) familial dysautonomia [Riley-Day] (G90.1) | |
Q85.0 | Neurofibromatosis (nonmalignant) | |
Q85.00 | Neurofibromatosis, unspecified | |
Q85.01 | Neurofibromatosis, type 1 | |
Info: | Von Recklinghausen disease | |
Q85.02 | Neurofibromatosis, type 2 | |
Info: | Acoustic neurofibromatosis | |
Q85.03 | Schwannomatosis | |
Q85.09 | Other neurofibromatosis | |
Q85.1 | Tuberous sclerosis | |
Info: | Bourneville's disease Epiloia | |
Q85.8 | Other phakomatoses, not elsewhere classified | |
Excl1.: | Meckel-Gruber syndrome (Q61.9) | |
Q85.81 | PTEN tumor syndrome | |
Info: | PHTS PTEN hamartoma tumor syndrome PTEN related Cowden syndrome | |
Use add'l | , if applicable, genetic susceptibility to malignant neoplasm (Z15.0-) | |
Q85.82 | Other Cowden syndrome | |
Q85.83 | Von Hippel-Lindau syndrome | |
Use add'l | manifestations | |
Q85.89 | Other phakomatoses, not elsewhere classified | |
Info: | Peutz-Jeghers syndrome Sturge-Weber(-Dimitri) syndrome | |
Q85.9 | Phakomatosis, unspecified | |
Info: | Hamartosis NOS | |
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