F79
BillableUnspecified intellectual disabilities
Unspecified intellectual disabilities
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Mental deficiency NOS
- Mental subnormality NOS
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(305)
SNOMED CT
- 11p partial monosomy syndrome4135001
- Micrognathia-glossoptosis syndrome4602007
- Pierre Robin association4602007
- Pierre Robin syndrome4602007
- Robin sequence4602007
- Brachycephaly13649004
- Short anteroposterior diameter of skull13649004
- Short broad skull13649004
- Wide skull13649004
- Eyes wide apart22006008
- Eyes widely set22006008
- Hypertelorism22006008
- Orbital hypertelorism22006008
- Orbital separation excessive22006008
- Glossoplegia38228000
- Paralysis of tongue38228000
- Cracked tongue52368004
- Fissured tongue52368004
- Furrowed tongue52368004
- Lingua plicata52368004
- Plicated tongue52368004
- Scrotal tongue52368004
- Arachnodactyly62250003
- Congenital arachnodactyly62250003
- Spider finger62250003
- Micromelia74370006
- Micromelic dwarf74370006
- Micromelus74370006
- Nanomelia74370006
- Athetoid cerebral palsy75019001
- Congenital hepatic fibrosis79607001
- Intellectual developmental disorder110359009
- Intellectual disability110359009
- Blood magnesium abnormal166745009
- Blood magnesium outside reference range166745009
- Congenital fissure of tongue204631004
- Congenital plicated tongue204631004
- Intellectual functioning disability228156007
- Intellectual limitation228156007
- Congenital nuclear ophthalmoplegia230530003
- Dyskinetic cerebral palsy230780007
- POF - Premature ovarian failure237788002
- Premature ovarian failure237788002
- Below average intellect247575000
- Below average intelligence247575000
- Low intelligence247578003
- Combined malformation of central nervous system and skeletal muscle277949001
- Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Ohdo blepharophimosis syndrome412787009
- Extrapyramidal cerebral palsy702314005
- Non-spastic cerebral palsy702314005
- Chromosome 11p13 deletion syndrome715215007
- WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome715215007
- WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome715215007
- WAGR syndrome715215007
- Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome715215007
- Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome715215007
- Disorder of sex development with intellectual disability syndrome719450007
- Pseudohermaphroditism with intellectual disability syndrome719450007
- Verloes Gillerot Fryns syndrome719450007
- Arachnodactyly with abnormal ossification and intellectual disability syndrome720501007
- Kosztolanyi syndrome720501007
- Arachnodactyly and intellectual disability with facial dysmorphism syndrome720502000
- De Die, Smulders, Vles, Fryns syndrome720502000
- Cantalamessa Baldini Ambrosi syndrome721841001
- Hypogonadism with mitral valve prolapse and intellectual disability syndrome721841001
- Al Gazali Nair syndrome722110003
- Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome722110003
- Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome722454003
- Mental retardation syndrome Belgian type722454003
- Microcephaly, seizure, intellectual disability, heart disease syndrome723304001
- Deletion of part of chromosome 11726381002
- Deletion of part of chromosome 21726398002
- Intellectual developmental disorder due to nutritional deficiency763626009
- Intellectual disability due to nutritional deficiency763626009
- Intellectual disability, polydactyly, uncombable hair syndrome763742008
- Kozlowski Krajewska syndrome763742008
- Intellectual disability, brachydactyly, Pierre Robin syndrome763744009
- Intellectual disability Wolff type763745005
- Wolff Zimmermann syndrome763745005
- Cryptorchidism, arachnodactyly, intellectual disability syndrome764950001
- Van Benthem Driessen Hanveld syndrome764950001
- Brachydactyly, mesomelia, intellectual disability, heart defect syndrome765761009
- Stratton Garcia Young syndrome765761009
- ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder766824003
- Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder766824003
- Helsmoortel-van der Aa syndrome766824003
- Lundberg syndrome770679002
- Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome770679002
- Intellectual disability, seizures, macrocephaly, obesity syndrome770750002
- Kagami Ogata syndrome770907002
- Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect770907002
- Intellectual disability, short stature, hypertelorism syndrome771077007
- Stoll Geraudel Chauvin syndrome771077007
- Hepatic fibrosis, renal cyst, intellectual disability syndrome771149000
- Thompson Baraitser syndrome771149000
- White Sutton syndrome772127009
- CTCF-related neurodevelopmental disorder773552008
- Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome773552008
- FOXP1 syndrome774203000
- FOXP1-related intellectual disability, severe speech delay, mild dysmorphism syndrome774203000
- Intellectual disability, severe speech delay, mild dysmorphism syndrome774203000
- Levic Stefanovic Nikolic syndrome782945001
- Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome782945001
- Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome783005002
- 21q22.13q22.2 microdeletion syndrome783619003
- DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion783619003
- Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion783619003
- Monosomy 21q22.13q22.2783619003
- Curatolo Cilio Pessagno syndrome783703004
- White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome783703004
- Blepharophimosis, intellectual disability syndrome788584007
- Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language without loss of previously acquired skills870262000
- Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills870262000
- Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language with loss of previously acquired skills870265003
- Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills870265003
- Mesomelic dysplasia of upper limb1010609002
- Congenital dysplasia of radius1142185008
- Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome1169355000
- ZTTK syndrome1169355000
- Zhu Tokita Takenouchi Kim syndrome1169355000
- DYRK1A (dual specificity tyrosine phosphorylation regulated kinase 1A)-related intellectual disability syndrome1179301003
- DYRK1A syndrome1179301003
- DYRK1A-related intellectual disability syndrome1179301003
- Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome1179301003
- Blood magnesium below reference range1179460004
- Primary hypomagnesaemia, generalised seizures, intellectual disability, obesity syndrome1351854006
- Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome1351854006
- Genetic syndromic childhood obesity1359763002
UMLS
- DEFIC MENTALC0917816
- Deficiencies, MentalC0917816
- Deficiency mentalC0917816
- Deficiency, MentalC0917816
- MENTAL DEFICC0917816
- Mental DeficienciesC0917816
- Mental DeficiencyC0917816
- Mental deficiencyC0917816
- Mental deficiency NOSC0917816
- mental deficienciesC0917816
- mental deficiencyC0917816
- Mental disabilityC1306341
- Mental disability NOSC1306341
- Mental handicap NOSC1306341
- Mental impairmentC1306341
- Mental impairment NOSC1306341
- Mental subnormality NOSC1306341
- disabilities mentalC1306341
- handicap mentalC1306341
- handicapped mentalC1306341
- handicaps mentalC1306341
- mental disabilityC1306341
- mental handicapC1306341
- mental subnormalityC1306341
- Unspecified intellectual disabilitiesC3161331
Clinical Terms
- Hepatic fibrosis, renal cyst, intellectual disability syndrome
- Mental disability
- Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome
- Mental retardation syndrome Belgian type
- Mental Deficiency
- ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder
- Hypogonadism with mitral valve prolapse and intellectual disability syndrome
- Lingua plicata
- Al Gazali Nair syndrome
- Plicated tongue
- Micromelus
- disabilities mental
- mental deficiencies
- mental handicap
- Orbital separation excessive
- Paralysis of tongue
- Premature ovarian failure
- mental subnormality
- Arachnodactyly
- Brachycephaly
- DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
- Congenital plicated tongue
- handicaps mental
- Micromelic dwarf
- WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome
- Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome
- Below average intellect
- FOXP1-related intellectual disability, severe speech delay, mild dysmorphism syndrome
- Non-spastic cerebral palsy
- Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language without loss of previously acquired skills
- Pseudohermaphroditism with intellectual disability syndrome
- Kagami Ogata syndrome
- ZTTK syndrome
- Intellectual disability due to nutritional deficiency
- Intellectual disability, short stature, hypertelorism syndrome
- Intellectual functioning disability
- Mental impairment
- Ohdo blepharophimosis syndrome
- Eyes wide apart
- Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome
- Spider finger
- Arachnodactyly and intellectual disability with facial dysmorphism syndrome
- Helsmoortel-van der Aa syndrome
- Thompson Baraitser syndrome
- 11p partial monosomy syndrome
- Short anteroposterior diameter of skull
- Blood magnesium abnormal
- Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
- Microcephaly, seizure, intellectual disability, heart disease syndrome
- Low intelligence
- Fissured tongue
- Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills
- Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome
- Furrowed tongue
- Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
- Congenital dysplasia of radius
- Robin sequence
- Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language with loss of previously acquired skills
- Intellectual developmental disorder due to nutritional deficiency
- Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
- Chromosome 11p13 deletion syndrome
- Intellectual developmental disorder
- Mental deficiency NOS
- Congenital arachnodactyly
- Mesomelic dysplasia of upper limb
- Intellectual disability, polydactyly, uncombable hair syndrome
- WAGR syndrome
- handicap mental
- Below average intelligence
- Intellectual disability
- FOXP1 syndrome
- Short broad skull
- Van Benthem Driessen Hanveld syndrome
- Congenital nuclear ophthalmoplegia
- Mental subnormality NOS
- Stratton Garcia Young syndrome
- Orbital hypertelorism
- Primary hypomagnesaemia, generalised seizures, intellectual disability, obesity syndrome
- Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
- Zhu Tokita Takenouchi Kim syndrome
- Wide skull
- Eyes widely set
- Intellectual disability, severe speech delay, mild dysmorphism syndrome
- De Die, Smulders, Vles, Fryns syndrome
- Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder
- Verloes Gillerot Fryns syndrome
- Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome
- POF - Premature ovarian failure
- White Sutton syndrome
- Congenital fissure of tongue
- Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome
- Arachnodactyly with abnormal ossification and intellectual disability syndrome
- Intellectual disability Wolff type
- Intellectual limitation
- Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
- Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome
- Mental disability NOS
- Deficiencies, Mental
- Deletion of part of chromosome 11
- Cantalamessa Baldini Ambrosi syndrome
- Curatolo Cilio Pessagno syndrome
- Hypertelorism
- Disorder of sex development with intellectual disability syndrome
- Combined malformation of central nervous system and skeletal muscle
- Cracked tongue
- Blood magnesium below reference range
- Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
- Monosomy 21q22.13q22.2
- Scrotal tongue
- Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills
- Stoll Geraudel Chauvin syndrome
- Genetic syndromic childhood obesity
- DYRK1A syndrome
- Pierre Robin association
- Intellectual disability, brachydactyly, Pierre Robin syndrome
- Wolff Zimmermann syndrome
- Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
- Mental handicap NOS
- Dyskinetic cerebral palsy
- WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome
- Deficiency, Mental
- Micromelia
- Cryptorchidism, arachnodactyly, intellectual disability syndrome
- DEFIC MENTAL
- Blepharophimosis, intellectual disability syndrome
- White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome
- DYRK1A (dual specificity tyrosine phosphorylation regulated kinase 1A)-related intellectual disability syndrome
- Deficiency mental
- DYRK1A-related intellectual disability syndrome
- handicapped mental
- Deletion of part of chromosome 21
- Glossoplegia
- Extrapyramidal cerebral palsy
- Lundberg syndrome
- Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome
- Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
- Kosztolanyi syndrome
- MENTAL DEFIC
- 21q22.13q22.2 microdeletion syndrome
- Athetoid cerebral palsy
- Pierre Robin syndrome
- Micrognathia-glossoptosis syndrome
- Levic Stefanovic Nikolic syndrome
- Nanomelia
- CTCF-related neurodevelopmental disorder
- Blood magnesium outside reference range
- Congenital hepatic fibrosis
- Intellectual disability, seizures, macrocephaly, obesity syndrome
- Kozlowski Krajewska syndrome
- Mental impairment NOS
Frequently Asked Questions
What is the ICD-10 code for unspecified intellectual disabilities?
The ICD-10-CM code for unspecified intellectual disabilities is F79. The full clinical description is "Unspecified intellectual disabilities". F79 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code F79 mean?
ICD-10-CM code F79 represents “Unspecified 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 F79 a billable code?
Yes, F79 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is F79 in?
F79 is in Chapter 5: Mental, Behavioral and Neurodevelopmental Disorders (codes F01-F99).
What codes cannot be used with F79?
F79 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 F79 map to?
F79 maps to 61 SNOMED CT concepts: 4135001, 783619003, 766824003, 722110003, 62250003, and 56 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for F79?
F79 is linked to 3 UMLS Concept Unique Identifiers: C0917816, C1306341, C3161331. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does F79 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like unspecified 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 F79?
F79 maps to the ICD-11 code: 6A00.Z (Disorders of intellectual development, unspecified).
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.