R62.50
BillableUnsp lack of expected normal physiol dev in childhood
Unspecified lack of expected normal physiological development in childhood
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)
Also Known As / Clinical Terms
SNOMED CT
- Micrognathia-glossoptosis syndrome4602007
- Pierre Robin association4602007
- Pierre Robin syndrome4602007
- Robin sequence4602007
- 10p partial monosomy syndrome6002006
- Familial visceral neuropathy20725005
- Neonatal diabetes mellitus49817004
- Pentose disorder57507002
- Big jaw72855002
- Congenital prognathism72855002
- Exognathia72855002
- Progenia72855002
- Prognathia72855002
- Prognathism72855002
- Problem of growth and development85456006
- Fallot's tetralogy86299006
- Subpulmonic stenosis, ventricular septal defect, overriding aorta, AND right ventricular hypertrophy86299006
- TOF - Tetralogy of Fallot86299006
- Tetralogy of Fallot86299006
- Body weight AND/OR growth problem105722002
- False anodontia109440005
- Amino acid below reference range124057005
- Decreased amino acid124057005
- Delayed growth and development129815002
- Childhood growth AND/OR development alteration129823000
- Severe combined immunodeficiency with low T- and B-cell numbers190997006
- Tooth absent234948008
- Tooth missing234948008
- Developmental delay248290002
- Child developmental finding251803000
- Child developmental observation251803000
- Physiological development failure274626005
- Body growth problem301329004
- Finding of infant milestone302088004
- Observation of infant milestones302088004
- Altered growth and development409033001
- Growth and development alteration409033001
- Inadequate maintenance of developmental tasks424379006
- Inadequate achievement of developmental tasks425301002
- Delay in physiological development447740001
- Fellman syndrome703388005
- Finnish lactic acidosis with hepatic hemosiderosis703388005
- Finnish lethal neonatal metabolic syndrome703388005
- GRACILE syndrome703388005
- Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death703388005
- Impaired child development704304000
- Impairment of child development704304000
- Impaired infant development704370008
- Impairment of infant development704370008
- Impaired newborn development704371007
- Impairment of newborn development704371007
- Impaired adolescent development704428004
- Impairment of adolescent development704428004
- Congenital heart defect with round face and developmental delay syndrome715987000
- Sonoda syndrome715987000
- Game Friedman Paradice syndrome716198008
- Growth delay with hydrocephalus and lung hypoplasia syndrome716198008
- Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome719833004
- Cernunnos-XLF deficiency720853005
- NHEJ1 (non-homologous end joining factor) syndrome720853005
- Severe combined immunodeficiency due to Cernunnos protein deficiency720853005
- Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionising radiation syndrome720853005
- Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome720853005
- DEND (developmental delay, epilepsy, neonatal diabetes) syndrome721088003
- DEND syndrome721088003
- Developmental delay, epilepsy, neonatal diabetes syndrome721088003
- GAPO (growth retardation, alopecia, pseudoanodontia, optic atrophy) syndrome721843003
- GAPO syndrome721843003
- Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome721843003
- Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome722051004
- Osteosclerosis, developmental delay, craniosynostosis syndrome722117000
- Foot contracture, muscle atrophy, oculomotor apraxia syndrome722456001
- Intellectual disability, developmental delay, contracture syndrome722456001
- Wieacker Wolff syndrome722456001
- Bindewald Ulmer Muller syndrome723336008
- Fallot complex with intellectual disability and growth delay syndrome723336008
- Deletion of part of chromosome 5726372008
- Deletion of part of long arm of chromosome 5726373003
- Deletion of part of chromosome 10726380001
- Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome733469003
- Hypo-and hypermelanotic cutaneous macules, retarded growth, intellectual disability syndrome733469003
- Westerhof Beemer Cormane syndrome733469003
- Congenital sideroblastic anaemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome765327005
- Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome765327005
- Congenital cataract, progressive muscular hypotonia, deafness, developmental delay syndrome773398005
- Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome773398005
- Congenital cataract, deafness, severe developmental delay syndrome773648002
- Congenital cataract, hearing loss, severe developmental delay syndrome773648002
- Lethal neurodegenerative disorder due to copper transport defect773648002
- FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome774070008
- Fibulin 1-related developmental delay, central nervous system anomaly, syndactyly syndrome774070008
- Growth retardation, mild developmental delay, chronic hepatitis syndrome774204006
- Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome774205007
- 10p12p11 microdeletion syndrome783061008
- Deletion 10p11.21p12.31783061008
- Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion783061008
- Facial dysmorphism, developmental delay, behavioural abnormalities syndrome due to 10p11.21p12.31 microdeletion783061008
- Monosomy 10p11.21p12.31783061008
- Absence of teeth1162783002
- Growth delay, intellectual disability, hepatopathy syndrome1186713004
- 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
- X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome1197588008
- 5q23 microdeletion syndrome1216940001
- Joint contractures, developmental delay, Pierre Robin syndrome1216940001
- Short stature, developmental delay, congenital heart defect syndrome1237512003
- TKT (transketolase) deficiency disorder1237512003
- Transketolase deficiency disorder1237512003
- GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder1260195002
- Glutamate ionotropic receptor NMDA type subunit 2B-related developmental delay, intellectual disability, autism spectrum disorder1260195002
- G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum1281842000
- GNAO1-related developmental delay, seizures, movement disorder spectrum1281842000
- GNAO1-related spectrum1281842000
- MYT1L-related Prader-Willi-like syndrome1303866001
- MYT1L-related developmental delay, intellectual disability, obesity syndrome1303866001
- Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome1303866001
- Developmental delay, epilepsy, neonatal diabetes syndrome, intermediate form1303868000
- Intermediate DEND (developmental delay, epilepsy, neonatal diabetes) syndrome1303868000
- Intermediate DEND syndrome1303868000
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation) syndrome1332508004
- CIMDAG (cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation) syndrome1332508004
- CIMDAG syndrome1332508004
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anaemia, growth retardation syndrome1332508004
- Cerebellar hypoplasia, intellectual disability, congenital microcephaly, dystonia, anemia, growth retardation syndrome1332508004
- Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome1340174002
- Developmental delay, immunodeficiency, leukoencephalopathy, hypohomocysteinemia syndrome1340174002
- Developmental delay, overweight, facial dysmorphism, behavioral abnormalities syndrome1340176000
- Developmental delay, overweight, facial dysmorphism, behavioural abnormalities syndrome1340176000
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.
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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.