G90.1
BillableFamilial dysautonomia [Riley-Day]
Familial dysautonomia [Riley-Day]
Coding Notes
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
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(9)
G90.0Idiopathic peripheral autonomic neuropathy
G90.2Horner's syndrome
G90.3Multi-system degeneration of the autonomic nervous system
G90.4Autonomic dysreflexia
G90.5Complex regional pain syndrome I (CRPS I)
G90.8Other disorders of autonomic nervous system
G90.9Disorder of the autonomic nervous system, unspecified
G90.APostural orthostatic tachycardia syndrome [POTS]
G90.BLMNB1-related autosomal dominant leukodystrophy
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(82)
SNOMED CT
- Dominant hereditary sensory neuropathy, type III29159009
- Familial dysautonomia29159009
- HSAN III29159009
- Hereditary sensory and autonomic neuropathy type III29159009
- Hereditary sensory and autonomic neuropathy, type III29159009
- Riley-Day syndrome29159009
- Hereditary dysautonomia with motor neuropathy230557001
- Lisker Garcia Ramos syndrome230557001
- Peripheral motor neuropathy dysautonomia syndrome230557001
UMLS
- DYSC0013364
- DYSAUTONOMIA, FAMILIALC0013364
- Dominant Hereditary Sensory Neuropathy, Type IIIC0013364
- Dominant hereditary sensory neuropathy, type IIIC0013364
- Dysautonomia, FamilialC0013364
- Familial DysautonomiaC0013364
- Familial dysautonomiaC0013364
- Familial dysautonomia (disorder)C0013364
- Familial dysautonomia [Riley-Day]C0013364
- HSAN (Hereditary Sensory and Autonomic Neuropathy) Type IIIC0013364
- HSAN 3C0013364
- HSAN IIIC0013364
- HSAN Type IIIC0013364
- HSAN type IIIC0013364
- HSAN3C0013364
- HSN-IIIC0013364
- Hereditary Sensory Neuropathy Type 3C0013364
- Hereditary Sensory Neuropathy, Dominant, Type 3C0013364
- Hereditary Sensory Neuropathy, Dominant, Type IIIC0013364
- Hereditary Sensory Neuropathy, Type 3, DominantC0013364
- Hereditary Sensory and Autonomic Neuropathy 3C0013364
- Hereditary Sensory and Autonomic Neuropathy Type IIIC0013364
- Hereditary sensory and autonomic neuropathy type IIIC0013364
- Hereditary sensory and autonomic neuropathy, type IIIC0013364
- Hereditary-Sensory and Autonomic Neuropathy Type IIIC0013364
- NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIIC0013364
- Neuropathy, Hereditary Sensory And Autonomic, Type IIIC0013364
- Neuropathy, Hereditary Sensory and Autonomic, Type IIIC0013364
- Neuropathy, Hereditary and Autonomic, Type IIIC0013364
- RILEY-DAY SYNDROMEC0013364
- Riley Day SyndromeC0013364
- Riley Day syndromeC0013364
- Riley-Day SyndromeC0013364
- Riley-Day syndromeC0013364
- Type 3 Hereditary Sensory Neuropathy, DominantC0013364
- Type III Hereditary Sensory Neuropathy, DominantC0013364
- dysautonomia familialC0013364
- familial autonomic nervous dysfunctionC0013364
- familial dysautonomiaC0013364
- riley day syndromeC0013364
- riley days syndromeC0013364
- riley-day syndromeC0013364
Clinical Terms
- HSAN (Hereditary Sensory and Autonomic Neuropathy) Type III
- HSN-III
- Type III Hereditary Sensory Neuropathy, Dominant
- Hereditary Sensory Neuropathy Type 3
- HSAN Type III
- Dysautonomia, Familial
- DYS
- Familial dysautonomia (disorder)
- Peripheral motor neuropathy dysautonomia syndrome
- HSAN 3
- dysautonomia familial
- HSAN3
- NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III
- Riley-Day Syndrome
- HSAN III
- riley day syndrome
- Hereditary sensory and autonomic neuropathy, type III
- Dominant Hereditary Sensory Neuropathy, Type III
- familial autonomic nervous dysfunction
- Hereditary sensory and autonomic neuropathy type III
- Hereditary Sensory Neuropathy, Dominant, Type III
- Hereditary-Sensory and Autonomic Neuropathy Type III
- Hereditary Sensory Neuropathy, Type 3, Dominant
- Hereditary Sensory Neuropathy, Dominant, Type 3
- Hereditary Sensory and Autonomic Neuropathy 3
- Lisker Garcia Ramos syndrome
- Neuropathy, Hereditary and Autonomic, Type III
- Familial Dysautonomia
- Hereditary dysautonomia with motor neuropathy
- riley days syndrome
- Type 3 Hereditary Sensory Neuropathy, Dominant
Frequently Asked Questions
What is the ICD-10 code for familial dysautonomia [riley-day]?
The ICD-10-CM code for familial dysautonomia [riley-day] is G90.1. The full clinical description is "Familial dysautonomia [Riley-Day]". G90.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G90.1 mean?
ICD-10-CM code G90.1 represents “Familial dysautonomia [Riley-Day]”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G90.1 a billable code?
Yes, G90.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G90.1 in?
G90.1 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G90.1?
G90.1 has Excludes1 notes indicating codes that cannot be used together with it, including: dysfunction of the autonomic nervous system due to alcohol (G31.2).
What SNOMED CT codes does G90.1 map to?
G90.1 maps to 2 SNOMED CT concepts: 29159009, 230557001. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G90.1?
G90.1 is linked to 1 UMLS Concept Unique Identifier: C0013364. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G90.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like familial dysautonomia [riley-day] affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of G90.1?
G90.1 maps to the ICD-11 code: 8C21.1 (Hereditary sensory and autonomic neuropathy type III).
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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.