1. ICD-10-CM Codes
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2. E00-E89
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3. E20-E35
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4. E34-
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5. 2023 ICD-10-CM Diagnosis Code E34.8

2023 ICD-10-CM Diagnosis Code E34.8

Other specified endocrine disorders

2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code

• E34.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
• The 2023 edition of ICD-10-CM E34.8 became effective on October 1, 2022.
• This is the American ICD-10-CM version of E34.8 - other international versions of ICD-10 E34.8 may differ.

• Cyst of pineal gland
• Hutchinson-gilford syndrome
• Pineal cyst
• Progeria syndrome

• A disease that produces rapid aging, beginning in childhood
• A very rare genetic disorder caused by mutations in the lmna gene. It is characterized by premature aging. Signs and symptoms include failure to thrive, limited growth, alopecia, wrinkled skin, small face, development of atherosclerosis, and heart disease. There is no cure for this condition. Individuals do not usually survive beyond their early twenties. Death usually occurs as a result of complications from atherosclerosis.
• An abnormal congenital condition, associated with defects in the lamin type a gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature greying; hair loss; hearing loss (deafness); cataracts (cataract); arthritis; osteoporosis; diabetes mellitus; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary hyaluronic acid; and accelerated atherosclerosis. Many affected individuals develop malignant tumors, especially sarcoma.

• 643 Endocrine disorders with mcc
• 644 Endocrine disorders with cc
• 645 Endocrine disorders without cc/mcc

Convert E34.8 to ICD-9-CM

• 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
• 2017 (effective 10/1/2016): No change
• 2018 (effective 10/1/2017): No change
• 2019 (effective 10/1/2018): No change
• 2020 (effective 10/1/2019): No change
• 2021 (effective 10/1/2020): No change
• 2022 (effective 10/1/2021): No change
• 2023 (effective 10/1/2022): No change

• Type 1 Excludes: E34.3
  , E79
  , E79
  ICD-10-CM Diagnosis Code E34.3

  Short stature due to endocrine disorder

  2016 2017 2018 2019 2020 2021 2022 2023 - Converted to Parent Code Non-Billable/Non-Specific Code

  Type 1 Excludes

  • achondroplastic short stature (Q77.4)
  • hypochondroplastic short stature (Q77.4)
  • nutritional short stature (E45)
  • pituitary short stature (E23.0)
  • progeria (E34.8)
  • renal short stature (N25.0)
  • Russell-Silver syndrome (Q87.19)
  • short-limbed stature with immunodeficiency (D82.2)
  • short stature (child) (R62.52)
  • short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
  • short stature NOS (R62.52)
  ICD-10-CM Diagnosis Code E79

  Disorders of purine and pyrimidine metabolism

  2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code

  Type 1 Excludes

  • Ataxia-telangiectasia (Q87.19)
  • Bloom's syndrome (Q82.8)
  • Cockayne's syndrome (Q87.19)
  • calculus of kidney (N20.0)
  • combined immunodeficiency disorders (D81.-)
  • Fanconi's anemia (D61.09)
  • gout (M1A.-, M10.-)
  • orotaciduric anemia (D53.0)
  • progeria (E34.8)
  • Werner's syndrome (E34.8)
  • xeroderma pigmentosum (Q82.1)
  ICD-10-CM Diagnosis Code E79

  Disorders of purine and pyrimidine metabolism

  2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code

  Type 1 Excludes

  • Ataxia-telangiectasia (Q87.19)
  • Bloom's syndrome (Q82.8)
  • Cockayne's syndrome (Q87.19)
  • calculus of kidney (N20.0)
  • combined immunodeficiency disorders (D81.-)
  • Fanconi's anemia (D61.09)
  • gout (M1A.-, M10.-)
  • orotaciduric anemia (D53.0)
  • progeria (E34.8)
  • Werner's syndrome (E34.8)
  • xeroderma pigmentosum (Q82.1)

• Calcification
  • pineal gland E34.8
• Cyst (colloid) (mucous) (simple) (retention)
  • epiphysis cerebri E34.8
• Degeneration, degenerative
  • pineal gland E34.8
• Disease, diseased - see also Syndrome
  • pineal gland E34.8
• Donohue's syndrome E34.8
• Dysfunction
  • pineal gland E34.8
• Gilford-Hutchinson disease E34.8
• Hutchinson-Gilford disease or syndrome E34.8
• Hyperpinealism E34.8
• Hypopinealism E34.8
• Leprechaunism E34.8
• Pellizzi's syndrome E34.8
• Premature - see also condition
  • aging E34.8
  • senility E34.8
• Presenile - see also condition
  • premature aging E34.8
• Progeria E34.8
• Puberty (development state) Z00.3
  ICD-10-CM Diagnosis Code Z00.3

  Encounter for examination for adolescent development state

  2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Pediatric Dx (0-17 years) POA Exempt

  Applicable To

  • Encounter for puberty development state
  • premature E30.1
    ICD-10-CM Diagnosis Code E30.1

    Precocious puberty

    2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Pediatric Dx (0-17 years)

    Applicable To

    • Precocious menstruation

    Type 1 Excludes

    • Albright (-McCune) (-Sternberg) syndrome (Q78.1)
    • central precocious puberty (E22.8)
    • congenital adrenal hyperplasia (E25.0)
    • female heterosexual precocious pseudopuberty (E25.-)
    • male isosexual precocious pseudopuberty (E25.-)
    • due to
      • pineal tumor E34.8
• Senile, senility R41.81
  - see also condition
  ICD-10-CM Diagnosis Code R41.81

  Age-related cognitive decline

  2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Adult Dx (15-124 years)

  Applicable To

  • Senility NOS
  • premature E34.8
• Syndrome - see also Disease
  • pineal E34.8
  • premature senility E34.8
  • Werner's E34.8
• Werner's disease or syndrome E34.8

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.