R41.843
BillablePsychomotor deficit
Psychomotor deficit
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
Code First
The underlying condition must be sequenced before this code
- the underlying condition, if known, such as:
- •schizophreniaF20
Related Codes(4)
Also Known As / Clinical Terms(65)
SNOMED CT
- Impaired psychomotor development2806008
- Hypermethioninaemia43123004
- Hypermethioninemia43123004
- Disorder of zinc metabolism46727001
- Psychiatric sign or symptom53686002
- Agenesis of iris69278003
- Aniridia69278003
- Aplasia of iris69278003
- Congenital absence of iris69278003
- Congenital aniridia69278003
- Irideraemia69278003
- Irideremia69278003
- Congenital absence of the kidney204942005
- Renal agenesis204942005
- Psychotic symptom finding279315008
- Psychotic symptom observation279315008
- Motor retardation398991009
- Impaired psychomotor performance416909000
- Hypermethioninaemia due to S-adenosylhomocysteine hydrolase deficiency724039002
- Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency724039002
- Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency724039002
- Psychomotor symptom co-occurrent and due to psychotic disorder724759008
- Psychomotor symptom with psychotic disorder724759008
- Aniridia, renal agenesis, psychomotor retardation syndrome733116005
- Sommer Rathbun Battles syndrome733116005
- Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome782886007
- Autosomal recessive cerebellar ataxia, psychomotor delay syndrome783060009
- Autosomal recessive spinocerebellar ataxia type 11783060009
- Psychomotor retardation1144814003
- Cerebrorenal syndrome Perez type1187043002
- Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome1187043002
- Cognitive deficit in psychomotor function142291000119107
Clinical Terms
- Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome
- Irideremia
- Disorder of zinc metabolism
- Psychotic symptom finding
- Psychotic symptom observation
- Autosomal recessive spinocerebellar ataxia type 11
- Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
- Psychomotor retardation
- Agenesis of iris
- Congenital absence of the kidney
- Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome
- Renal agenesis
- Cognitive deficit in psychomotor function
- Psychomotor symptom co-occurrent and due to psychotic disorder
- Impaired psychomotor development
- Psychiatric sign or symptom
- Motor retardation
- Aniridia, renal agenesis, psychomotor retardation syndrome
- Hypermethioninaemia
- Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency
- Cerebrorenal syndrome Perez type
- Aplasia of iris
- Sommer Rathbun Battles syndrome
- Psychomotor symptom with psychotic disorder
- Aniridia
- Congenital absence of iris
- Irideraemia
- Impaired psychomotor performance
- Hypermethioninemia
- Hypermethioninaemia due to S-adenosylhomocysteine hydrolase deficiency
- Congenital aniridia
- Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency
Frequently Asked Questions
What is the ICD-10 code for psychomotor deficit?
The ICD-10-CM code for psychomotor deficit is R41.843. The full clinical description is "Psychomotor deficit". R41.843 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code R41.843 mean?
ICD-10-CM code R41.843 represents “Psychomotor deficit”. It is classified under Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings and is a billable/specific code that can be used on a claim.
Is R41.843 a billable code?
Yes, R41.843 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is R41.843 in?
R41.843 is in Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings (codes R00-R99).
What codes cannot be used with R41.843?
R41.843 has Excludes1 notes indicating codes that cannot be used together with it, including: dissociative [conversion] disorders (F44.-); mild cognitive impairment of uncertain or unknown etiology (G31.84); cognitive deficits as sequelae of cerebrovascular disease (I69.01-, I69.11-, I69.21-, I69.31-, I69.81-, I69.91-).
What SNOMED CT codes does R41.843 map to?
R41.843 maps to 17 SNOMED CT concepts: 69278003, 733116005, 783060009, 1187043002, 142291000119107, and 12 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for R41.843?
R41.843 is linked to 1 UMLS Concept Unique Identifier: C2921139. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does R41.843 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like psychomotor deficit 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 R41.843?
There is no direct ICD-11 mapping available for R41.843 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.