F88
BillableOther disorders of psychological development
Other disorders of psychological development
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Developmental agnosia
- Global developmental delay
- Other specified neurodevelopmental disorder
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
- Inherited disorder of folate metabolism4702003
- Congenital aplastic anaemia28975000
- Congenital aplastic anemia28975000
- Constitutional aplastic anaemia28975000
- Constitutional aplastic anemia28975000
- Hypoplastic anaemia - familial28975000
- Hypoplastic anemia - familial28975000
- Autism, childhood onset43614003
- Autistic disorder of childhood onset43614003
- Childhood autism43614003
- Cortical blindness68574006
- Mixed disorder of psychological development192147004
- Global developmental delay224958001
- Slow to talk229721007
- Speech delay229721007
- Developmental agnosia231537008
- Disorder of ornithine metabolism237928008
- Ornithine metabolism disorder237928008
- Dysplasia with defective mineralisation254117007
- Dysplasia with defective mineralization254117007
- Excessive eating267023007
- Gluttony267023007
- Hyperphagia267023007
- Polyphagia267023007
- Finding of quantity of eating289142005
- Observation of quantity of eating289142005
- Nephroblastoma302849000
- Wilm's tumor302849000
- Wilms tumor302849000
- Wilms tumour302849000
- Mixed developmental disorder442059001
- Developmental regression609225004
- Global developmental delay, osteopenia, ectodermal defect syndrome717813005
- HSAN (hereditary sensory and autonomic neuropathy) with deafness and global delay717826009
- Hereditary sensory and autonomic neuropathy with deafness and global delay717826009
- Der Kaloustian McIntosh Silver syndrome721883006
- Radioulnar synostosis with developmental delay and hypotonia syndrome721883006
- Ossification anomaly with psychomotor developmental delay syndrome722107005
- Developmental delay with autism spectrum disorder and gait instability770790004
- CTCF-related neurodevelopmental disorder773552008
- Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome773552008
- BBIS - Beaulieu Boycott Innes syndrome773554009
- Beaulieu Boycott Innes syndrome773554009
- THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome773554009
- THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome773554009
- Pancytopenia with developmental delay syndrome774071007
- Trilineage bone marrow failure with developmental delay syndrome774071007
- Growth retardation, mild developmental delay, chronic hepatitis syndrome774204006
- GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome782722002
- GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome782722002
- GLOW syndrome782722002
- Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome782722002
- Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome782722002
- Developmental delay due to ALDH6A1 (aldehyde dehydrogenase 6 family member A1) deficiency782828005
- Developmental delay due to MMSDH (methylmalonate semialdehyde dehydrogenase) deficiency782828005
- Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency782828005
- Developmental delay, facial dysmorphism syndrome due to MED13L deficiency787093004
- Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency787093004
- Hypoplasia of distal phalanx of hand1145503000
- Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome1172630000
- Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome1172696009
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome1172900005
- Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome1187042007
- SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures1187277001
- Short stature, brachydactyly, obesity, global developmental delay syndrome1187277001
- PLAA-associated neurodevelopmental disorder1217367007
- PLAAND - phospholipase A2 activating protein-associated neurodevelopmental disorder1217367007
- Phospholipase A2 activating protein-associated neurodevelopmental disorder1217367007
- Baker Gordon syndrome1217371005
- Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome1217371005
- SYT1-related neurodevelopmental disorder1217371005
- Synaptotagmin 1-related neurodevelopmental disorder1217371005
- GPAA1-related biosynthesis defect1217381009
- Glycosylphosphatidylinositol anchor attachment 1-related biosynthesis defect1217381009
- Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome1217381009
- Pierpont syndrome1220594007
- Plantar lipomatosis, facial dysmorphism, developmental delay syndrome1220594007
- Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome1222655009
- Bachmann Bupp syndrome1222658006
- Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome1222658006
- Ornithine decarboxylase deficiency1222658006
- TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome1222708006
- Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome1222708006
- X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome1237420004
- Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome1260140008
- Congenital radioulnar synostosis1268409009
- MTHFS (methenyltetrahydrofolate synthetase) related developmental delay, microcephaly, short stature, epilepsy syndrome1300128003
- MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome1300128003
- Methenyltetrahydrofolate synthetase-related developmental delay, microcephaly, short stature, epilepsy syndrome1300128003
- NRXN1(neurexin 1) related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance1300131002
- NRXN1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance1300131002
- Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance1300131002
- IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome1303273003
- Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome1303273003
- Early-onset obesity, hyperphagia, severe developmental delay syndrome1303867005
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome with combined immunodeficiency due to diaphanous related formin 1 mutation1354858008
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 deficiency1354858008
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation1354858008
- SCBMS (seizures, cortical blindness, microcephaly syndrome) with combined immunodeficiency due to DIAPH1 mutation1354858008
- HAFOUS - Hao Fountain syndrome1360075006
- Hao Fountain syndrome1360075006
- Hereditary cerebellar atrophy431641000124107
- Severe obesity83911000119104
UMLS
- Agnosia, DevelopmentalC0395013
- Agnosias, DevelopmentalC0395013
- Developmental AgnosiaC0395013
- Developmental AgnosiasC0395013
- Developmental agnosiaC0395013
- Developmental agnosia (disorder)C0395013
- Delayed cognitive developmentC0557874
- Delayed developmentC0557874
- Delayed developmental milestonesC0557874
- Delayed intellectual developmentC0557874
- Delayed milestonesC0557874
- Delayed psychomotor developmentC0557874
- Developmental delayC0557874
- Developmental delay in early childhoodC0557874
- Developmental delay, globalC0557874
- Developmental retardationC0557874
- GDDC0557874
- Global developmental delayC0557874
- Global developmental delay (disorder)C0557874
- Lack of psychomotor developmentC0557874
- Motor and developmental delayC0557874
- Motormental retardationC0557874
- No psychomotor developmentC0557874
- Psychomotor delayC0557874
- Psychomotor development deficiencyC0557874
- Psychomotor development failureC0557874
- Psychomotor developmental delayC0557874
- Retarded developmentC0557874
- Retarded mental developmentC0557874
- Retarded psychomotor developmentC0557874
- global developmental delayC0557874
- Other disorders of psychological developmentC0478657
- Other specified neurodevelopmental disorderC4237334
Frequently Asked Questions
What is ICD-10 code F88?
ICD-10-CM code F88 represents "Other disorders of psychological development". It is a billable/specific code that can be used on a claim.
Is F88 a billable code?
Yes, F88 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is F88 in?
F88 is in Chapter 5: Mental, Behavioral and Neurodevelopmental Disorders (codes F01-F99).
What SNOMED CT codes does F88 map to?
F88 maps to 51 SNOMED CT concepts: 43614003, 773554009, 1222658006, 1217371005, 773552008, and 46 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for F88?
F88 is linked to 4 UMLS Concept Unique Identifiers: C0395013, C0557874, C0478657, C4237334. 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.