F89
BillableUnspecified disorder of psychological development
Unspecified disorder of psychological development
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
- symptoms, signs and abnormal clinical laboratory findings, not elsewhere classified (R00-R99)
Also Known As / Clinical Terms
SNOMED CT
- Achondrogenesis2391001
- Developmental disorder5294002
- Macroencephaly9740002
- Megalencephaly9740002
- Pili torti17170005
- Twisted hair17170005
- Developmental disorder of hyperkinesis46745001
- Hyperkinetic syndrome with developmental delay46745001
- Axonal neuropathy60703000
- Cortical blindness68574006
- Achondroplasia86268005
- Achondroplastic dwarf86268005
- Achondroplastic dwarfism86268005
- Chondrodystrophia fetalis86268005
- Congenital osteosclerosis86268005
- Osteosclerosis congenita86268005
- Developmental mental disorder129104009
- Hyperkinesis with developmental delay192131001
- Disorder of psychological development192562009
- Slow to talk229721007
- Speech delay229721007
- Megakaryocytic thrombocytopenia234483004
- Immuno-osseous dysplasia254067002
- Malabsorption of glucose267426009
- Developmental hereditary disorder363070008
- Acanthosis nigricans402599005
- Developmentally disabled443656000
- Left ventricular myocardial noncompaction cardiomyopathy447935001
- Ventricular myocardial noncompaction cardiomyopathy471875005
- Neurodevelopmental disorder700364009
- Pili torti with developmental delay and neurological abnormality syndrome716194005
- Early childhood developmental disability716710007
- Early developmental impairment716710007
- Tic due to developmental disorder722973009
- Secondary neurodevelopmental disorder737343009
- Insulin resistance763325000
- Autism spectrum disorder with disorder of intellectual development and impaired functional language870305003
- Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language870305003
- Autism spectrum disorder with disorder of intellectual development and complete impairment of functional language870308001
- Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language870308001
- SADDAN (severe achondroplasia, developmental delay, acanthosis nigricans) syndrome874931001
- Severe achondroplasia, developmental delay, acanthosis nigricans syndrome874931001
- Neurodevelopmental disorder due to maternal use of alcohol1003385006
- Harel Yoon syndrome1172586007
- Ocular anomalies, axonal neuropathy, developmental delay syndrome1172586007
- Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome1172624000
- RERE-related neurodevelopmental syndrome1172624000
- TELO2-related intellectual disability, neurodevelopmental disorder1172626003
- Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder1172626003
- You Hoover Fong syndrome1172626003
- Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Takenouchi Kosaki syndrome1172685001
- Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome1172839002
- Palatal anomalies, multiple diastemata, facial dysmorphism, developmental delay syndrome1172889005
- Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome1172889005
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome1172900005
- EXTL3 (exostosin like glycosyltransferase 3) related neuro-immuno-skeletal dysplasia syndrome1177175008
- EXTL3-related neuro-immuno-skeletal dysplasia syndrome1177175008
- Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 (exostosin like glycosyltransferase 3) deficiency1177175008
- Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 deficiency1177175008
- Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome1177175008
- Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract1179282009
- CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome1179408008
- Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome1179408008
- Snijders Blok-Campeau syndrome1179408008
- Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome1187212004
- WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome1187247007
- WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome1187247007
- WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome1187247007
- WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome1187247007
- SPPRS (spastic paraplegia, psychomotor retardation, seizures) syndrome1187278006
- Spastic paraplegia, severe developmental delay, epilepsy syndrome1187278006
- MINDS (macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax) syndrome1187304005
- MINDS syndrome1187304005
- Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome1187304005
- Smith Kingsmore syndrome1187304005
- Microcephalic primordial dwarfism, insulin resistance syndrome1220596009
- Au Kline syndrome1222710008
- Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome1222710008
- Okamoto syndrome1222710008
- CNTNAP2 developmental and epileptic encephalopathy1230376005
- CNTNAP2-DEE - CNTNAP2 developmental and epileptic encephalopathy1230376005
- CNTNAP2-related developmental and epileptic encephalopathy1230376005
- Contactin associated protein 2-related developmental and epileptic encephalopathy1230376005
- Cortical dysplasia, focal epilepsy syndrome1230376005
- CLIFAHDD (congenital limbs, face contractures, hypotonia, developmental delay) syndrome1255322002
- CLIFAHDD syndrome1255322002
- Congenital contracture of limbs and face, hypotonia, developmental delay syndrome1255322002
- Cerebellar ataxia, brain abnormalities, cardiac conduction defects syndrome1303586006
- Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome1303586006
- Neurodevelopmental delay, hypotonia, cerebellar atrophy, cardiac conduction defects syndrome1303586006
- CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome1332384001
- Cyclin K-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome1332384001
- CHD4-related neurodevelopmental disorder1332510002
- CHD4-related neurodevelopmental syndrome1332510002
- Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder1332510002
- Sifrim Hitz Weiss syndrome1332510002
- OGIN syndrome1356735003
- Oculogastrointestinal neurodevelopmental syndrome1356735003
- Body height below reference range1363478003
- DHX30-related neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome1363573005
- DHX30-related neurodevelopmental disorder1363573005
- Neurodevelopmental delay, intellectual disability, ataxia, feeding difficulty syndrome1363573005
UMLS
- CHILD DEVELOPMENT DISC0008073
- Child Development DisorderC0008073
- Child Development DisordersC0008073
- DEVELOPMENT DIS CHILDC0008073
- Development Disorder, ChildC0008073
- Development Disorders, ChildC0008073
- Developmental DisabilitiesC0008073
- Developmental DisabilityC0008073
- Developmental DisorderC0008073
- Developmental disabilityC0008073
- Developmental disorderC0008073
- Developmental disorder (disorder)C0008073
- Developmental disorder NOSC0008073
- Disabilities, DevelopmentalC0008073
- Disability, DevelopmentalC0008073
- child development disorderC0008073
- child development disordersC0008073
- child developmental disabilitiesC0008073
- developmental delay disordersC0008073
- developmental disabilitiesC0008073
- developmental disabilityC0008073
- developmental disorderC0008073
- developmental disordersC0008073
- Child Mental DisorderC1535926
- Child Mental DisordersC1535926
- Disorder, Child MentalC1535926
- Disorder, NeurodevelopmentalC1535926
- Mental Disorder, ChildC1535926
- Mental Disorders Diagnosed in ChildhoodC1535926
- Mental Disorders Usually Diagnosed in Infancy, Childhood or AdolescenceC1535926
- Mental Disorders, ChildC1535926
- Neurodevelopmental DisorderC1535926
- Neurodevelopmental DisordersC1535926
- Neurodevelopmental Disorders Usually Diagnosed in Infancy, Childhood or AdolescenceC1535926
- Neurodevelopmental disorderC1535926
- Neurodevelopmental disorder (disorder)C1535926
- Neurodevelopmental disorder NOSC1535926
- Neurodevelopmental disordersC1535926
- Neurodevelopmental impairmentC1535926
- Social-emotional developmental delayC1535926
- Disorder of psychological developmentC0478658
- Disorder of psychological development (disorder)C0478658
- Unspecified disorder of psychological developmentC0478658
- disorders of psychological developmentC0478658
Frequently Asked Questions
What is ICD-10 code F89?
ICD-10-CM code F89 represents "Unspecified disorder of psychological development". It 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.
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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.