AutoICD API

R62.50

Billable

Unsp lack of expected normal physiol dev in childhood

Unspecified lack of expected normal physiological development in childhood

Status

Billable / Specific

Block

R50-R69

Parent Code

R62.5

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Infantilism NOS

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

Related Codes(3)
R62.51

Failure to thrive (child)

BillableR62.52

Short stature (child)

BillableR62.59

Oth lack of expected normal physiol development in childhood

Billable
Also Known As / Clinical Terms(269)

SNOMED CT

UMLS

Clinical Terms

  • Growth delay with hydrocephalus and lung hypoplasia syndrome
  • Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionising radiation syndrome
  • Deletion of part of long arm of chromosome 5
  • Developmental delay, overweight, facial dysmorphism, behavioural abnormalities syndrome
  • Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome
  • GAPO syndrome
  • Congenital cataract, progressive muscular hypotonia, deafness, developmental delay syndrome
  • Physiological development failure
  • Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form
  • GRACILE syndrome
  • Finnish lactic acidosis with hepatic hemosiderosis
  • Exognathia
  • Childhood growth AND/OR development alteration
  • Finding of infant milestone
  • GAPO (growth retardation, alopecia, pseudoanodontia, optic atrophy) syndrome
  • Fellman syndrome
  • Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome
  • Altered growth and development
  • Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation syndrome
  • Impaired infant development
  • Infantilism
  • Impairment of adolescent development
  • Big jaw
  • Transketolase deficiency disorder
  • Severe combined immunodeficiency due to Cernunnos protein deficiency
  • Intermediate DEND (developmental delay, epilepsy, neonatal diabetes) syndrome
  • Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
  • 10p12p11 microdeletion syndrome
  • 10p partial monosomy syndrome
  • Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome
  • Hypo-and hypermelanotic cutaneous macules, retarded growth, intellectual disability syndrome
  • DEND (developmental delay, epilepsy, neonatal diabetes) syndrome
  • Impairment of newborn development
  • WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • MYT1L-related developmental delay, intellectual disability, obesity syndrome
  • Progenia
  • Deletion of part of chromosome 10
  • Growth and development alteration
  • Problem of growth and development
  • Congenital prognathism
  • GNAO1-related spectrum
  • Wieacker Wolff syndrome
  • False anodontia
  • Pentose disorder
  • Congenital cataract, hearing loss, severe developmental delay syndrome
  • Westerhof Beemer Cormane syndrome
  • Robin sequence
  • WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome
  • Observation of infant milestones
  • CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation) syndrome
  • WAC-related facial dysmorphism, developmental delay, behavioural abnormalities syndrome
  • X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome
  • Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome
  • Fallot complex with intellectual disability and growth delay syndrome
  • GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder
  • Impairment of infant development
  • MYT1L-related Prader-Willi-like syndrome
  • Subpulmonic stenosis, ventricular septal defect, overriding aorta, AND right ventricular hypertrophy
  • Cernunnos-XLF deficiency
  • Growth retardation, mild developmental delay, chronic hepatitis syndrome
  • Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
  • Short stature, developmental delay, congenital heart defect syndrome
  • NHEJ1 (non-homologous end joining factor) syndrome
  • Delay in physiological development
  • Prognathism
  • Inadequate maintenance of developmental tasks
  • Tooth missing
  • Child developmental observation
  • Impaired child development
  • Osteosclerosis, developmental delay, craniosynostosis syndrome
  • Bindewald Ulmer Muller syndrome
  • Monosomy 10p11.21p12.31
  • Congenital sideroblastic anaemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
  • Absence of teeth
  • Body growth problem
  • Growth delay, intellectual disability, hepatopathy syndrome
  • Amino acid below reference range
  • Impaired adolescent development
  • Body weight AND/OR growth problem
  • Prognathia
  • Finnish lethal neonatal metabolic syndrome
  • CIMDAG syndrome
  • Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome
  • G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum
  • Neonatal diabetes mellitus
  • Severe combined immunodeficiency with low T- and B-cell numbers
  • Tetralogy of Fallot
  • Inadequate achievement of developmental tasks
  • Game Friedman Paradice syndrome
  • 5q23 microdeletion syndrome
  • WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
  • TOF - Tetralogy of Fallot
  • Delayed growth and development
  • Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
  • CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation) syndrome
  • Fallot's tetralogy
  • Infantilism NOS
  • Deletion of part of chromosome 5
  • Congenital cataract, deafness, severe developmental delay syndrome
  • Developmental delay
  • Pierre Robin association
  • Deletion 10p11.21p12.31
  • Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome
  • Lethal neurodegenerative disorder due to copper transport defect
  • Child developmental finding
  • Decreased amino acid
  • Congenital heart defect with round face and developmental delay syndrome
  • Familial visceral neuropathy
  • Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
  • Intellectual disability, developmental delay, contracture syndrome
  • FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
  • Foot contracture, muscle atrophy, oculomotor apraxia syndrome
  • Developmental delay, overweight, facial dysmorphism, behavioral abnormalities syndrome
  • Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death
  • Infantilism (disorder)
  • GNAO1-related developmental delay, seizures, movement disorder spectrum
  • Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome
  • Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder
  • Intermediate DEND syndrome
  • Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome
  • Developmental delay, epilepsy, neonatal diabetes syndrome
  • TKT (transketolase) deficiency disorder
  • Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion
  • Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
  • Impairment of child development
  • Impaired newborn development
  • Pierre Robin syndrome
  • Micrognathia-glossoptosis syndrome
  • DEND syndrome
  • Sonoda syndrome
  • Tooth absent
  • Joint contractures, developmental delay, Pierre Robin syndrome
  • Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome
Frequently Asked Questions
What is the ICD-10 code for unsp lack of expected normal physiol dev in childhood?

The ICD-10-CM code for unsp lack of expected normal physiol dev in childhood is R62.50. The full clinical description is "Unspecified lack of expected normal physiological development in childhood". R62.50 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code R62.50 mean?

ICD-10-CM code R62.50 represents “Unspecified lack of expected normal physiological development in childhood”. It is classified under Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings and is a billable/specific code that can be used on a claim.

Is R62.50 a billable code?

Yes, R62.50 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is R62.50 in?

R62.50 is in Chapter 18: Symptoms, Signs and Abnormal Clinical and Laboratory Findings (codes R00-R99).

What codes cannot be used with R62.50?

R62.50 has Excludes1 notes indicating codes that cannot be used together with it, including: delayed puberty (E30.0); gonadal dysgenesis (Q99.1); hypopituitarism (E23.0); and 2 more.

What SNOMED CT codes does R62.50 map to?

R62.50 maps to 63 SNOMED CT concepts: 6002006, 783061008, 1216940001, 1162783002, 409033001, and 58 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for R62.50?

R62.50 is linked to 2 UMLS Concept Unique Identifiers: C0175948, C0878753. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does R62.50 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like unsp lack of expected normal physiol dev in childhood 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 R62.50?

There is no direct ICD-11 mapping available for R62.50 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.