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Diagnosis Code

E34.8 OTHER SPECIFIED ENDOCRINE DISORDERS


Code Information

Diagnosis Code: E34.8

Short Description: Other specified endocrine disorders

Long Description: Other specified endocrine disorders

The code E34.8 is VALID for claim submission

Code Classification:

  • Endocrine, nutritional and metabolic diseases (E00–E89)
    • Disorders of other endocrine glands (E20-E35)
      • Other endocrine disorders (E34)
        • E34.8 Other specified endocrine disorders

Code Version: 2022 ICD-10-CM


Synonyms

  • Abnormal corticosterone
  • Abnormal estradiol
  • Abnormal serotonin
  • Abnormality of serotonin secretion
  • Acrogeria
  • Acroosteolysis
  • Acroosteolysis, keloid-like lesions, premature aging syndrome
  • Aging
  • Atypical Werner syndrome
  • Autoimmune endocrine disease
  • Calcification of pineal gland
  • Complex gonadal endocrine disorder
  • Congenital anomaly of subcutaneous tissue
  • Diabetes mellitus due to genetic defect in insulin action
  • Diabetes mellitus due to genetic defect in insulin action
  • Disorder of androgen receptor
  • Disorder of endocrine gonad
  • Endocrine alopecia
  • Endocrine andrology disorder
  • Endocrine axis dysfunction
  • Euthyroid Graves orbitopathy
  • General adaptation syndrome
  • Glucose-galactose malabsorption
  • Gynecological endocrinology disorder
  • Hereditary acroosteolysis
  • Hutchinson-Gilford syndrome
  • Hypothalamic-pituitary-adrenal axis dysfunction
  • Hypothalamic-pituitary-gonadal axis dysfunction
  • Hypothalamic-pituitary-gonadal axis dysfunction
  • Hypothalamic-pituitary-ovarian axis dysfunction
  • Hypothalamic-pituitary-testicular axis dysfunction
  • Insulin biosynthesis defect
  • Insulin receptor defect
  • Insulin resistance
  • Laminopathy with premature aging
  • Laminopathy with premature aging
  • Laminopathy with premature aging
  • Laminopathy with premature aging
  • Leprechaunism syndrome
  • LMNA-related cardiocutaneous progeria syndrome
  • Macrogenitosomia
  • Macrogenitosomia praecox due to pineal disorder
  • Malabsorption of glucose
  • Mandibular hypoplasia, deafness, progeroid syndrome
  • Marfan's syndrome
  • Mass of endocrine structure
  • Metageria
  • Multiple malformation syndrome with senile-like appearance
  • Neonatal pseudo-hydrocephalic progeroid syndrome
  • Nestor Guillermo progeria syndrome
  • Pineal degeneration
  • Pineal gland disorder
  • Pineal gland dysfunction
  • Premature aging
  • Premature aging syndrome
  • Progeroid and marfanoid aspect, lipodystrophy syndrome
  • Progeroid features, hepatocellular carcinoma predisposition syndrome
  • Progeroid short stature with pigmented nevi
  • Progeroid syndrome Petty type
  • Rabson-Mendenhall syndrome
  • Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
  • Werner syndrome

Diagnostic Related Group(s)

The code E34.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Endocrine Disorders With Mcc (643)
  • Endocrine Disorders With Cc (644)
  • Endocrine Disorders Without Cc/mcc (645)

References to Index of Diseases and Injuries

The code E34.8 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Pineal gland dysfunction
    • Progeria
  • Type 2 Excludes Notes:
    • pseudohypoparathyroidism (@E20.1*)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
E34.8 Right Arrow 259.8 Endocrine disorders NEC

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
E34 Other endocrine disorders
E34.0 Carcinoid syndrome
E34.1 Other hypersecretion of intestinal hormones
E34.2 Ectopic hormone secretion, not elsewhere classified
E34.3 Short stature due to endocrine disorder
E34.30 Short stature due to endocrine disorder, unspecified
E34.31 Constitutional short stature
E34.32 Genetic causes of short stature
E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency
E34.322 Insulin-like growth factor-1 (IGF-1) resistance
E34.328 Other genetic causes of short stature
E34.329 Unspecified genetic causes of short stature
E34.39 Other short stature due to endocrine disorder
E34.4 Constitutional tall stature
E34.5 Androgen insensitivity syndrome
E34.50 Androgen insensitivity syndrome, unspecified
E34.51 Complete androgen insensitivity syndrome
E34.52 Partial androgen insensitivity syndrome
E34.9 Endocrine disorder, unspecified

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

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