AutoICD API

F88

Billable

Other disorders of psychological development

Other disorders 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 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

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(267)

SNOMED CT

UMLS

Clinical Terms

  • Autism, childhood onset
  • Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome with combined immunodeficiency due to diaphanous related formin 1 mutation
  • Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency
  • HAFOUS - Hao Fountain syndrome
  • Hypoplastic anemia - familial
  • GLOW syndrome
  • NRXN1(neurexin 1) related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance
  • Global developmental delay (disorder)
  • Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome
  • Inherited disorder of folate metabolism
  • Bachmann Bupp syndrome
  • Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome
  • MTHFS (methenyltetrahydrofolate synthetase) related developmental delay, microcephaly, short stature, epilepsy syndrome
  • Pancytopenia with developmental delay syndrome
  • Developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency
  • Developmental delay, global
  • Trilineage bone marrow failure with developmental delay syndrome
  • Hyperphagia
  • Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome
  • Phospholipase A2 activating protein-associated neurodevelopmental disorder
  • BBIS - Beaulieu Boycott Innes syndrome
  • Disorder of ornithine metabolism
  • Speech delay
  • Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome
  • Motormental retardation
  • NRXN1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance
  • X-linked intellectual disability, global development delay, facial dysmorphism, sacral caudal remnant syndrome
  • Early-onset obesity, hyperphagia, severe developmental delay syndrome
  • Developmental delay in early childhood
  • Hereditary cerebellar atrophy
  • Wilms tumor
  • Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome
  • TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome
  • Dysplasia with defective mineralization
  • HSAN (hereditary sensory and autonomic neuropathy) with deafness and global delay
  • GDD
  • Motor and developmental delay
  • Delayed developmental milestones
  • Delayed cognitive development
  • Developmental delay due to ALDH6A1 (aldehyde dehydrogenase 6 family member A1) deficiency
  • Pierpont syndrome
  • Retarded psychomotor development
  • PLAA-associated neurodevelopmental disorder
  • Developmental delay due to MMSDH (methylmalonate semialdehyde dehydrogenase) deficiency
  • Dysplasia with defective mineralisation
  • Congenital radioulnar synostosis
  • Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome
  • SYT1-related neurodevelopmental disorder
  • Growth retardation, mild developmental delay, chronic hepatitis syndrome
  • Beaulieu Boycott Innes syndrome
  • Wilms tumour
  • Wilm's tumor
  • Agnosia, Developmental
  • Radioulnar synostosis with developmental delay and hypotonia syndrome
  • Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome
  • Constitutional aplastic anemia
  • Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance
  • Hypoplasia of distal phalanx of hand
  • Retarded development
  • Hao Fountain syndrome
  • PLAAND - phospholipase A2 activating protein-associated neurodevelopmental disorder
  • Other specified neurodevelopmental disorder
  • Ornithine metabolism disorder
  • Baker Gordon syndrome
  • IRF2BPL-related regressive neurodevelopmental disorder, dystonia, seizures syndrome
  • Global developmental delay
  • Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
  • Developmental Agnosias
  • Global developmental delay, osteopenia, ectodermal defect syndrome
  • Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome
  • THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
  • Excessive eating
  • Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation
  • Delayed development
  • Gluttony
  • Agnosias, Developmental
  • Delayed psychomotor development
  • Developmental Agnosia
  • Psychomotor development deficiency
  • Mixed disorder of psychological development
  • Retarded mental development
  • Childhood autism
  • Polyphagia
  • Developmental retardation
  • SCBMS (seizures, cortical blindness, microcephaly syndrome) with combined immunodeficiency due to DIAPH1 mutation
  • Delayed milestones
  • Psychomotor developmental delay
  • No psychomotor development
  • THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome
  • Autistic disorder of childhood onset
  • Developmental agnosia (disorder)
  • Developmental delay with autism spectrum disorder and gait instability
  • Psychomotor development failure
  • Ossification anomaly with psychomotor developmental delay syndrome
  • Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 deficiency
  • Hereditary sensory and autonomic neuropathy with deafness and global delay
  • Developmental delay, facial dysmorphism syndrome due to MED13L deficiency
  • SBIDDS - short stature, brachydactyly, impaired intellectual development, seizures
  • Developmental delay
  • Methenyltetrahydrofolate synthetase-related developmental delay, microcephaly, short stature, epilepsy syndrome
  • GPAA1-related biosynthesis defect
  • Synaptotagmin 1-related neurodevelopmental disorder
  • Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome
  • MTHFS-related developmental delay, microcephaly, short stature, epilepsy syndrome
  • Developmental regression
  • Delayed intellectual development
  • Nephroblastoma
  • Finding of quantity of eating
  • Lack of psychomotor development
  • Observation of quantity of eating
  • Severe obesity
  • Constitutional aplastic anaemia
  • Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome
  • Plantar lipomatosis, facial dysmorphism, developmental delay syndrome
  • Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome
  • Mixed developmental disorder
  • Short stature, brachydactyly, obesity, global developmental delay syndrome
  • Ornithine decarboxylase deficiency
  • Congenital aplastic anaemia
  • Cortical blindness
  • Glycosylphosphatidylinositol anchor attachment 1-related biosynthesis defect
  • GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome
  • Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome
  • Psychomotor delay
  • Slow to talk
  • Der Kaloustian McIntosh Silver syndrome
  • CTCF-related neurodevelopmental disorder
  • GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome
  • Hypoplastic anaemia - familial
  • Congenital aplastic anemia
  • Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome
Frequently Asked Questions
What is the ICD-10 code for other disorders of psychological development?

The ICD-10-CM code for other disorders of psychological development is F88. The full clinical description is "Other disorders of psychological development". F88 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code F88 mean?

ICD-10-CM code F88 represents “Other disorders 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 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.

How does F88 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders 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 F88?

F88 maps to the ICD-11 code: 6A0Z (Neurodevelopmental disorders, unspecified).

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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.