Diagnosis Code: R62.50

Short Description: Unsp lack of expected normal physiol dev in childhood

Long Description: Unspecified lack of expected normal physiological development in childhood

The code R62.50 is VALID for claim submission

Code Classification:

• Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00–R99)
  • General symptoms and signs (R50-R69)
    • Lack of expected normal physiol dev in childhood and adults (R62)
      • R62.50 Unsp lack of expected normal physiol dev in childhood

Code Version: 2022 ICD-10-CM

Synonyms

• 10p partial monosomy syndrome
• Absence of teeth
• Altered growth and development
• Body growth problem
• Body weight AND/OR growth problem
• Body weight AND/OR growth problem
• Child developmental finding
• Child developmental finding
• Child developmental finding
• Childhood growth AND/OR development alteration
• Congenital cataract, hearing loss, severe developmental delay syndrome
• Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
• Congenital prognathism
• Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome
• Delay in physiological development
• Delayed growth and development
• Deletion of part of chromosome 10
• Deletion of part of chromosome 5
• Deletion of part of long arm of chromosome 5
• DEND syndrome
• Developmental delay
• Facial dysmorphism, developmental delay, behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion
• Fallot complex with intellectual disability and growth delay syndrome
• False anodontia
• Familial visceral neuropathy
• FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome
• Finding of infant milestone
• Finding of infant milestone
• Game Friedman Paradice syndrome
• GAPO syndrome
• GRACILE syndrome
• Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome
• Growth delay, intellectual disability, hepatopathy syndrome
• Growth retardation, mild developmental delay, chronic hepatitis syndrome
• Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
• Impairment of adolescent development
• Impairment of child development
• Impairment of infant development
• Impairment of newborn development
• Inadequate achievement of developmental tasks
• Inadequate maintenance of developmental tasks
• Intellectual disability, developmental delay, contracture syndrome
• Joint contractures, developmental delay, Pierre Robin syndrome
• Neonatal diabetes mellitus
• Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome
• Osteosclerosis, developmental delay, craniosynostosis syndrome
• Pentose disorder
• Physiological development failure
• Problem of growth and development
• Robin sequence
• Severe combined immunodeficiency with low T- and B-cell numbers
• Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome
• Short stature, developmental delay, congenital heart defect syndrome
• Sonoda syndrome
• Tetralogy of Fallot
• Tooth absent
• Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
• WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
• X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome

Diagnostic Related Group(s)

The code R62.50 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Miscellaneous Disorders Of Nutrition, Metabolism, Fluids And Electrolytes With Mcc (640)
• Miscellaneous Disorders Of Nutrition, Metabolism, Fluids And Electrolytes Without Mcc (641)

References to Index of Diseases and Injuries

The code R62.50 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Infantilism NOS

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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