AutoICD API

E34.8

Billable

Other specified endocrine disorders

Other specified endocrine disorders

Status

Billable / Specific

Block

E20-E35

Parent Code

E34

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Pineal gland dysfunction
  • Progeria

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(7)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(269)

SNOMED CT

Clinical Terms

  • Abnormality of serotonin secretion
  • Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
  • Genetic syndromes of diabetes mellitus
  • Premature ageing syndrome
  • Pineal hyperplasia AND diabetes mellitus syndrome
  • hutchinson gilford syndrome
  • Euthyroid Graves ophthalmopathy
  • Progeroid syndrome Petty type
  • Hutchinson-Gilford Progeria Syndromes
  • Atypical progeroid syndrome
  • Laminopathy with premature aging
  • Disorder of pineal gland
  • PROGERIA
  • Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome
  • Euthyroid Graves eye disease
  • Pineal gland calcification
  • Mass of endocrine structure
  • Progeria Syndromes, Hutchinson-Gilford
  • Disorder of endocrine gonad
  • General adaptation syndrome
  • Multiple malformation syndrome with senile-like appearance
  • Acroosteolysis
  • Baraitser syndrome
  • Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome
  • Hutchinson-Gilford syndrome (disorder)
  • Mulvihill-Smith syndrome
  • Premature aging syndrome
  • Stress syndrome
  • Endocrine andrology disorder
  • Euthyroid Graves orbitopathy
  • Hypothalamic-pituitary-gonadal axis dysfunction
  • Macrogenitosomia praecox due to pineal disorder
  • Adult premature aging syndrome
  • Hutchinson-Gilford Disease
  • Acrogeria
  • Progeria Syndrome, Hutchinson-Gilford
  • Macrogenitosomia
  • Disorder of serotonin
  • Mandibular hypoplasia, deafness, progeroid syndrome
  • Selye's syndrome
  • Diabetes mellitus associated with genetic syndrome
  • Calcification of pineal gland
  • Leprechaunism
  • Physiologically old for age
  • Mendenhall syndrome
  • Atypical Werner syndrome
  • Adult progeria
  • Premature senility syndrome
  • Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities
  • Hypothalamic-pituitary-ovarian axis dysfunction
  • Progeria syndrome
  • Abnormal serotonin
  • Progeroid short stature with pigmented nevi
  • Laminopathy with premature ageing
  • Adult premature ageing syndrome
  • Diabetes mellitus due to genetic defect in insulin action
  • Gottron's syndrome
  • Marfan's syndrome
  • Leprechaunism syndrome
  • Progeria of the adult
  • NGPS - Nestor Guillermo progeria syndrome
  • Pineal gland dysfunction (disorder)
  • Euthyroid Graves' eye disease
  • Premature aging
  • HGPS
  • Nestor Guillermo progeria syndrome
  • Ageing
  • Insulin resistance
  • HUTCHINSON-GILFORD PROGERIA SYNDROME
  • Insulin receptor defect
  • Pangeria
  • Petty syndrome
  • Donohue's syndrome
  • Hutchinson Gilford Progeria Syndrome
  • Abnormal oestradiol
  • Donohue syndrome
  • Premature ageing syndrome Penttinen type
  • Abnormal corticosterone
  • Complex gonadal endocrine disorder
  • LMNA-related cardiocutaneous progeria syndrome
  • Progeroid features, hepatocellular carcinoma predisposition syndrome
  • Abnormality of 5-hydroxytryptamine secretion
  • Aging
  • Rabson-Mendenhall syndrome
  • Marfan's disease
  • Degeneration of pineal gland
  • Metageria
  • Hypothalamic-pituitary-testicular axis dysfunction
  • Marfan syndrome
  • Petty Laxova Wiedemann syndrome
  • Pineal gland degeneration
  • Congenital anomaly of subcutaneous tissue
  • Premature ageing
  • MDP (mandibular hypoplasia, deafness, progeroid) syndrome
  • Progeroid short stature with pigmented naevi
  • Acroosteolysis, keloid-like lesions, premature aging syndrome
  • Hypothalamic-pituitary-adrenal axis dysfunction
  • Pellizzi syndrome
  • Autoimmune endocrine disease
  • Macrogenitosomia praecox due to disorder of pineal gland
  • Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome
  • Insulin biosynthesis defect
  • Abnormal compound B
  • Disorder of estradiol
  • Progeroid and marfanoid aspect, lipodystrophy syndrome
  • Acroosteolysis, keloid-like lesions, premature ageing syndrome
  • Abnormal estradiol
  • Hereditary acroosteolysis
  • hutchinson-gilford syndrome
  • Disorder of oestradiol
  • Endocrine axis dysfunction
  • Wiedemann-Rautenstrauch syndrome
  • Pineal gland disorder
  • Lamin A/C related cardiocutaneous progeria syndrome
  • Endocrine alopecia
  • Malabsorption of glucose
  • Pineal gland dysfunction
  • Gynaecological endocrinology disorder
  • Gynecological endocrinology disorder
  • Androgen receptor abnormal
  • Werner syndrome
  • Disorder of androgen receptor
  • Ruijs Aalfs syndrome
  • Neonatal pseudo-hydrocephalic progeroid syndrome
  • Pineal degeneration
  • Premature aging syndrome, Penttinen type
  • Mandibular hypoplasia, hearing loss, progeroid syndrome
Frequently Asked Questions
What is the ICD-10 code for other specified endocrine disorders?

The ICD-10-CM code for other specified endocrine disorders is E34.8. The full clinical description is "Other specified endocrine disorders". E34.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E34.8 mean?

ICD-10-CM code E34.8 represents “Other specified endocrine disorders”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E34.8 a billable code?

Yes, E34.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E34.8 in?

E34.8 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E34.8?

E34.8 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 1 more.

What SNOMED CT codes does E34.8 map to?

E34.8 maps to 57 SNOMED CT concepts: 386780000, 131064004, 131138007, 237594007, 238872007, and 52 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E34.8?

E34.8 is linked to 3 UMLS Concept Unique Identifiers: C0033300, C0029793, C0271531. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E34.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified endocrine disorders 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 E34.8?

E34.8 maps to the ICD-11 code: 5B3Z (Endocrine diseases, unspecified).

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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.