F72
BillableSevere intellectual disabilities
Severe intellectual disabilities
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- IQ 20-25 to 35-40
- Severe mental subnormality
Includes
Conditions included under this code
- disorders of psychological development
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
- any associated physical or developmental disorders
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
- Bilateral paralysis6481005
- Diplegia6481005
- Severe intellectual development disorder40700009
- Severe intellectual disability40700009
- Severe mental retardation (I.Q. 20-34)40700009
- Severe mental retardation (Intelligence Quotient 20-34)40700009
- Spastic paralysis78403003
- Congenital retrognathism109515000
- Retrognathia109515000
- Retrognathism109515000
- Spastic diplegia281411007
- Recession of bone298358008
- Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome770751003
- Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome773419004
- Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome773419004
- Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome773551001
- IQSEC2 (IQ motif and Sec7 domain 2) related syndromic intellectual disability774149004
- IQSEC2-related syndromic intellectual disability774149004
- Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome774149004
- AP4 deficiency syndrome778011005
- Severe intellectual disability and progressive spastic paraplegia778011005
- CTNNB1 syndrome782723007
- Severe intellectual disability, progressive spastic diplegia syndrome782723007
- Congenital absence of pain with severe intellectual disability1237623009
- Congenital analgesia with severe intellectual disability1237623009
- Congenital insensitivity to pain with preserved temperature sensation1237623009
- Congenital insensitivity to pain with severe intellectual disability1237623009
- Congenital insensitivity to pain with severe non-progressive cognitive delay1237623009
- Craniosynostosis, microretrognathia, severe intellectual disability syndrome1269224009
UMLS
- Early and severe mental retardationC0036857
- Intellectual disability, severeC0036857
- Mental retardation, severeC0036857
- Mental retardation, severe in some patientsC0036857
- Mental retardation, severe,C0036857
- Severe intellectual development disorderC0036857
- Severe intellectual disabilitiesC0036857
- Severe intellectual disabilityC0036857
- Severe intellectual disability (disorder)C0036857
- Severe mental retardationC0036857
- Severe mental retardation (I.Q. 20-34)C0036857
- Severe mental retardation (Intelligence Quotient 20-34)C0036857
- Severe mental subnormalityC0036857
- severe mental retardationC0036857
- IQ 20-25 to 35-40C2874987
Clinical Terms
- severe mental retardation
- Severe intellectual disability and progressive spastic paraplegia
- Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome
- Recession of bone
- IQ 20-25 to 35-40
- IQSEC2-related syndromic intellectual disability
- Retrognathia
- Mental retardation, severe in some patients
- Diplegia
- Severe intellectual disability (disorder)
- Congenital absence of pain with severe intellectual disability
- Retrognathism
- Severe intellectual development disorder
- Severe mental retardation (I.Q. 20-34)
- Severe mental subnormality
- Congenital insensitivity to pain with severe intellectual disability
- CTNNB1 syndrome
- Early and severe mental retardation
- Spastic diplegia
- IQSEC2 (IQ motif and Sec7 domain 2) related syndromic intellectual disability
- AP4 deficiency syndrome
- Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome
- Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome
- Intellectual disability, severe
- Craniosynostosis, microretrognathia, severe intellectual disability syndrome
- Congenital insensitivity to pain with preserved temperature sensation
- Severe mental retardation (Intelligence Quotient 20-34)
- Bilateral paralysis
- Congenital insensitivity to pain with severe non-progressive cognitive delay
- Mental retardation, severe,
- Severe intellectual disability, progressive spastic diplegia syndrome
- Congenital analgesia with severe intellectual disability
- Spastic paralysis
- Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome
- Mental retardation, severe
- Congenital retrognathism
- Severe intellectual disability, short stature, behavioral abnormalities, facial dysmorphism syndrome
- Severe intellectual disability
Frequently Asked Questions
What is the ICD-10 code for severe intellectual disabilities?
The ICD-10-CM code for severe intellectual disabilities is F72. The full clinical description is "Severe intellectual disabilities". F72 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code F72 mean?
ICD-10-CM code F72 represents “Severe intellectual disabilities”. It is classified under Chapter 5: Mental, Behavioral and Neurodevelopmental Disorders and is a billable/specific code that can be used on a claim.
Is F72 a billable code?
Yes, F72 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is F72 in?
F72 is in Chapter 5: Mental, Behavioral and Neurodevelopmental Disorders (codes F01-F99).
What codes cannot be used with F72?
F72 has Excludes1 notes indicating codes that cannot be used together with it, including: borderline intellectual functioning, IQ above 70 to 84 (R41.83).
What SNOMED CT codes does F72 map to?
F72 maps to 14 SNOMED CT concepts: 778011005, 6481005, 782723007, 1237623009, 109515000, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for F72?
F72 is linked to 2 UMLS Concept Unique Identifiers: C0036857, C2874987. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does F72 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like severe intellectual disabilities 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 F72?
F72 maps to the ICD-11 code: 6A00.2 (Disorder of intellectual development, severe).
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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.