AutoICD API

F89

Billable

Unspecified disorder of psychological development

Unspecified disorder of psychological development

Status

Billable / Specific

Block

F80-F89

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Developmental disorder NOS
  • Neurodevelopmental disorder NOS

Includes

Conditions included under this code

  • disorders of psychological development

Excludes 2

Conditions not included here, but the patient may have both

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

6A0ZNeurodevelopmental disorders, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(283)

SNOMED CT

UMLS

Clinical Terms

  • Axonal neuropathy
  • Osteosclerosis congenita
  • Au Kline syndrome
  • Left ventricular myocardial noncompaction cardiomyopathy
  • OGIN syndrome
  • Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome
  • Cortical dysplasia, focal epilepsy syndrome
  • Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language
  • Severe achondroplasia, developmental delay, acanthosis nigricans syndrome
  • Mental Disorders, Child
  • Pili torti with developmental delay and neurological abnormality syndrome
  • Hyperkinesis with developmental delay
  • Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
  • Speech delay
  • Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome
  • Snijders Blok-Campeau syndrome
  • Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome
  • developmental disability
  • Developmental Disorder
  • Ocular anomalies, axonal neuropathy, developmental delay syndrome
  • CHD4-related neurodevelopmental syndrome
  • Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
  • Mental Disorder, Child
  • Harel Yoon syndrome
  • CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome
  • Achondroplastic dwarfism
  • TELO2-related intellectual disability, neurodevelopmental disorder
  • Disorder of psychological development
  • EXTL3 (exostosin like glycosyltransferase 3) related neuro-immuno-skeletal dysplasia syndrome
  • Ventricular myocardial noncompaction cardiomyopathy
  • Disorder of psychological development (disorder)
  • Twisted hair
  • Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome
  • Secondary neurodevelopmental disorder
  • Disorder, Neurodevelopmental
  • Sifrim Hitz Weiss syndrome
  • SPPRS (spastic paraplegia, psychomotor retardation, seizures) syndrome
  • WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • CHD4-related neurodevelopmental disorder
  • Developmentally disabled
  • Achondroplastic dwarf
  • Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome
  • Okamoto syndrome
  • CNTNAP2-DEE - CNTNAP2 developmental and epileptic encephalopathy
  • MINDS (macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax) syndrome
  • Megakaryocytic thrombocytopenia
  • Developmental Disabilities
  • RERE-related neurodevelopmental syndrome
  • Disorder, Child Mental
  • WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome
  • Microcephalic primordial dwarfism, insulin resistance syndrome
  • Autism spectrum disorder with disorder of intellectual development and impaired functional language
  • WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome
  • Hyperkinetic syndrome with developmental delay
  • Acanthosis nigricans
  • Neurodevelopmental disorders
  • Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome
  • Social-emotional developmental delay
  • child developmental disabilities
  • Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome
  • Developmental disorder of hyperkinesis
  • child development disorders
  • Achondroplasia
  • Early developmental impairment
  • Oculogastrointestinal neurodevelopmental syndrome
  • Development Disorder, Child
  • DHX30-related neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome
  • Palatal anomalies, multiple diastemata, facial dysmorphism, developmental delay syndrome
  • MINDS syndrome
  • Early childhood developmental disability
  • Child Development Disorder
  • Developmental disorder (disorder)
  • developmental delay disorders
  • Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome
  • Insulin resistance
  • Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language
  • Neurodevelopmental disorder (disorder)
  • Mental Disorders Diagnosed in Childhood
  • Body height below reference range
  • Congenital osteosclerosis
  • Cerebellar ataxia, brain abnormalities, cardiac conduction defects syndrome
  • Developmental hereditary disorder
  • Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome
  • Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
  • DHX30-related neurodevelopmental disorder
  • SADDAN (severe achondroplasia, developmental delay, acanthosis nigricans) syndrome
  • Disability, Developmental
  • developmental disorders
  • Developmental disorder NOS
  • Smith Kingsmore syndrome
  • CNTNAP2-related developmental and epileptic encephalopathy
  • Contactin associated protein 2-related developmental and epileptic encephalopathy
  • Macroencephaly
  • WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • You Hoover Fong syndrome
  • Takenouchi Kosaki syndrome
  • Development Disorders, Child
  • Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder
  • Developmental mental disorder
  • Achondrogenesis
  • Immuno-osseous dysplasia
  • Neurodevelopmental delay, hypotonia, cerebellar atrophy, cardiac conduction defects syndrome
  • Neurodevelopmental disorder
  • Neurodevelopmental disorder due to maternal use of alcohol
  • EXTL3-related neuro-immuno-skeletal dysplasia syndrome
  • Neurodevelopmental disorder NOS
  • Spastic paraplegia, severe developmental delay, epilepsy syndrome
  • CHILD DEVELOPMENT DIS
  • Child Mental Disorders
  • Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract
  • CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome
  • Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome
  • Child Mental Disorder
  • Malabsorption of glucose
  • Neurodevelopmental impairment
  • Tic due to developmental disorder
  • Neurodevelopmental Disorders Usually Diagnosed in Infancy, Childhood or Adolescence
  • CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome
  • Megalencephaly
  • disorders of psychological development
  • Disabilities, Developmental
  • CLIFAHDD syndrome
  • Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 (exostosin like glycosyltransferase 3) deficiency
  • Chondrodystrophia fetalis
  • Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome
  • Cortical blindness
  • Autism spectrum disorder with disorder of intellectual development and complete impairment of functional language
  • CNTNAP2 developmental and epileptic encephalopathy
  • Slow to talk
  • Mental Disorders Usually Diagnosed in Infancy, Childhood or Adolescence
  • Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder
  • DEVELOPMENT DIS CHILD
  • Pili torti
  • Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome
  • Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 deficiency
Frequently Asked Questions
What is the ICD-10 code for unspecified disorder of psychological development?

The ICD-10-CM code for unspecified disorder of psychological development is F89. The full clinical description is "Unspecified disorder of psychological development". F89 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code F89 mean?

ICD-10-CM code F89 represents “Unspecified disorder of psychological development”. 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 F89 a billable code?

Yes, F89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is F89 in?

F89 is in Chapter 5: Mental, Behavioral and Neurodevelopmental Disorders (codes F01-F99).

What SNOMED CT codes does F89 map to?

F89 maps to 54 SNOMED CT concepts: 402599005, 2391001, 86268005, 1172624000, 1222710008, and 49 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for F89?

F89 is linked to 3 UMLS Concept Unique Identifiers: C0008073, C1535926, C0478658. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does F89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like unspecified disorder of psychological development 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 F89?

F89 maps to the ICD-11 code: 6A0Z (Neurodevelopmental disorders, 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.

Try FreeView API Docs

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.