Q85.01
BillableNeurofibromatosis, type 1
Neurofibromatosis, type 1
Status
Billable / Specific
Parent Code
Q85.0Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Von Recklinghausen disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Multiple non-ossifying fibromatosis92824003
- NF1 - Neurofibromatosis type 192824003
- Neurofibromatosis 192824003
- Neurofibromatosis type 192824003
- Neurofibromatosis, peripheral type92824003
- Von Recklinghausen disease92824003
- Cafe au lait spots201281002
- Cafe-au-lait spots201281002
- Café au lait spot201281002
- Café au lait spots201281002
- Segmental neurofibromatosis254241004
- Axillary freckling due to neurofibromatosis403815003
- Multiple cafe-au-lait macules due to neurofibromatosis403816002
- Multiple café-au-lait macules due to neurofibromatosis403816002
- Multiple neurofibromas in neurofibromatosis403817006
- Elephantiasis neurofibromatosa403819009
- Legius syndrome703541007
- NFLS - neurofibromatosis type 1-like syndrome703541007
- Neurofibromatosis type 1-like syndrome703541007
- NFNS - Neurofibromatosis Noonan syndrome715344006
- Neurofibromatosis Noonan syndrome715344006
- Neurofibromatosis type 1 Noonan syndrome715344006
- Neurofibromatosis with Noonan phenotype715344006
- Deletion of part of chromosome 17726389000
- Deletion of part of long arm of chromosome 17733300002
- 17q11 deletion syndrome880093002
- Chromosome 17q11.2 deletion syndrome880093002
- Monosomy 17q11880093002
- Neurofibromatosis type 1 microdeletion syndrome880093002
- Segmental neurofibromatosis type 11010653007
- MNF1 - mosaic neurofibromatosis type 11304118001
- Mosaic neurofibromatosis type 11304118001
UMLS
- Molluscum FibrosumC0027831
- Molluscum fibrosumC0027831
- Multiple non-ossifying fibromatosisC0027831
- NEUROFIBROMATOSIS TYPE 1C0027831
- NEUROFIBROMATOSIS, PERIPHERAL TYPEC0027831
- NEUROFIBROMATOSIS, TYPE IC0027831
- NF1C0027831
- NF1 (Neurofibromatosis 1)C0027831
- NF1 - Neurofibromatosis type 1C0027831
- Neurofibromatoses, PeripheralC0027831
- Neurofibromatoses, Type IC0027831
- Neurofibromatosis 1C0027831
- Neurofibromatosis IC0027831
- Neurofibromatosis Type 1C0027831
- Neurofibromatosis Type IC0027831
- Neurofibromatosis type 1C0027831
- Neurofibromatosis type 1 (disorder)C0027831
- Neurofibromatosis, PeripheralC0027831
- Neurofibromatosis, Peripheral TypeC0027831
- Neurofibromatosis, Peripheral, NF 1C0027831
- Neurofibromatosis, Peripheral, NF1C0027831
- Neurofibromatosis, Type 1C0027831
- Neurofibromatosis, Type IC0027831
- Neurofibromatosis, peripheral typeC0027831
- Neurofibromatosis, type 1C0027831
- Neurofibromatosis, type 1 (von Recklinghausen's disease)C0027831
- Peripheral NeurofibromatosesC0027831
- Peripheral NeurofibromatosisC0027831
- Peripheral neurofibromatosisC0027831
- RECKLINGHAUSEN DIS OF NERVEC0027831
- RECKLINGHAUSENS DIS OF NERVEC0027831
- Recklinghausen Disease of NerveC0027831
- Recklinghausen Disease, NerveC0027831
- Recklinghausen disease, nerveC0027831
- Recklinghausen's Disease of NerveC0027831
- Recklinghausen's diseaseC0027831
- Recklinghausen's neurofibromatosisC0027831
- Recklinghausens Disease of NerveC0027831
- Type 1 NeurofibromatosisC0027831
- Type 1, NeurofibromatosisC0027831
- Type I NeurofibromatosesC0027831
- Type I, NeurofibromatosisC0027831
- VON RECKLINGHAUSEN DISC0027831
- VON RECKLINGHAUSEN DISEASEC0027831
- VON RECKLINGHAUSENS DISC0027831
- Von Recklinghausen DiseaseC0027831
- Von Recklinghausen diseaseC0027831
- Von Recklinghausen's disease (of nerve)C0027831
- disease recklinghausensC0027831
- neurofibromatosis 1C0027831
- neurofibromatosis iC0027831
- neurofibromatosis type 1C0027831
- neurofibromatosis type iC0027831
- recklinghausen diseaseC0027831
- recklinghausen's diseaseC0027831
- von Recklinghausen DiseaseC0027831
- von Recklinghausen's DiseaseC0027831
- von Recklinghausen's diseaseC0027831
- von Recklinghausens DiseaseC0027831
- von recklinghausen diseaseC0027831
- von recklinghausen's diseaseC0027831
- von recklinghausens diseaseC0027831
Frequently Asked Questions
What is the ICD-10 code for neurofibromatosis, type 1?
The ICD-10-CM code for neurofibromatosis, type 1 is Q85.01. The full clinical description is "Neurofibromatosis, type 1". Q85.01 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q85.01 mean?
ICD-10-CM code Q85.01 represents "Neurofibromatosis, type 1". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q85.01 a billable code?
Yes, Q85.01 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q85.01 in?
Q85.01 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q85.01?
Q85.01 has Excludes1 notes indicating codes that cannot be used together with it, including: ataxia telangiectasia [Louis-Bar] (G11.3); familial dysautonomia [Riley-Day] (G90.1).
What SNOMED CT codes does Q85.01 map to?
Q85.01 maps to 14 SNOMED CT concepts: 880093002, 403815003, 201281002, 726389000, 733300002, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q85.01?
Q85.01 is linked to 1 UMLS Concept Unique Identifier: C0027831. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.