E34.8
BillableOther specified endocrine disorders
Other specified endocrine disorders
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Pineal gland dysfunction
- Progeria
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- pseudohypoparathyroidism (E20.1)
Also Known As / Clinical Terms
SNOMED CT
- Insulin biosynthesis defect1771008
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Pineal gland dysfunction9526000
- Androgen receptor abnormal9979004
- Disorder of androgen receptor9979004
- Insulin receptor defect10680005
- Multiple malformation syndrome with senile-like appearance12674005
- Marfan syndrome19346006
- Marfan's disease19346006
- Marfan's syndrome19346006
- Acroosteolysis27201004
- Mendenhall syndrome33559001
- Pineal hyperplasia AND diabetes mellitus syndrome33559001
- Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities33559001
- Rabson-Mendenhall syndrome33559001
- Adult premature ageing syndrome51626007
- Adult premature aging syndrome51626007
- Adult progeria51626007
- Pangeria51626007
- Progeria of the adult51626007
- Werner syndrome51626007
- Endocrine alopecia54539003
- Congenital anomaly of subcutaneous tissue56759000
- Physiologically old for age88587007
- Premature ageing88587007
- Premature aging88587007
- Donohue syndrome111307005
- Donohue's syndrome111307005
- Leprechaunism111307005
- Leprechaunism syndrome111307005
- Complex gonadal endocrine disorder123757009
- Disorder of endocrine gonad127345001
- Disorder of pineal gland128470003
- Pineal gland disorder128470003
- General adaptation syndrome129632001
- Selye's syndrome129632001
- Stress syndrome129632001
- Abnormal estradiol131064004
- Abnormal oestradiol131064004
- Disorder of estradiol131064004
- Disorder of oestradiol131064004
- Abnormal serotonin131138007
- Disorder of serotonin131138007
- Abnormality of 5-hydroxytryptamine secretion237594007
- Abnormality of serotonin secretion237594007
- Gynaecological endocrinology disorder237786003
- Gynecological endocrinology disorder237786003
- Autoimmune endocrine disease237822008
- Hutchinson-Gilford syndrome238870004
- Premature senility syndrome238870004
- Progeria238870004
- Progeria syndrome238870004
- Metageria238871000
- Acrogeria238872007
- Gottron's syndrome238872007
- Neonatal pseudo-hydrocephalic progeroid syndrome238874008
- Wiedemann-Rautenstrauch syndrome238874008
- Ageing248280005
- Aging248280005
- Hereditary acroosteolysis254148004
- Malabsorption of glucose267426009
- Endocrine andrology disorder276856001
- Mass of endocrine structure300860002
- Abnormal compound B386780000
- Abnormal corticosterone386780000
- Baraitser syndrome399947002
- Mulvihill-Smith syndrome399947002
- Progeroid short stature with pigmented naevi399947002
- Progeroid short stature with pigmented nevi399947002
- Premature ageing syndrome399959003
- Premature aging syndrome399959003
- Endocrine axis dysfunction442498002
- Hypothalamic-pituitary-gonadal axis dysfunction442761002
- Hypothalamic-pituitary-adrenal axis dysfunction442762009
- Hypothalamic-pituitary-ovarian axis dysfunction442781001
- Hypothalamic-pituitary-testicular axis dysfunction442782008
- Diabetes mellitus due to genetic defect in insulin action609569007
- Atypical Werner syndrome715633008
- Atypical progeroid syndrome715633008
- Insulin resistance763325000
- Petty Laxova Wiedemann syndrome770567006
- Petty syndrome770567006
- Progeroid syndrome Petty type770567006
- NGPS - Nestor Guillermo progeria syndrome773331001
- Nestor Guillermo progeria syndrome773331001
- MDP (mandibular hypoplasia, deafness, progeroid) syndrome773406003
- Mandibular hypoplasia, deafness, progeroid syndrome773406003
- Mandibular hypoplasia, hearing loss, progeroid syndrome773406003
- LMNA-related cardiocutaneous progeria syndrome773426004
- Lamin A/C related cardiocutaneous progeria syndrome773426004
- Progeroid and marfanoid aspect, lipodystrophy syndrome773644000
- Acroosteolysis, keloid-like lesions, premature ageing syndrome776417008
- Acroosteolysis, keloid-like lesions, premature aging syndrome776417008
- Premature ageing syndrome Penttinen type776417008
- Premature aging syndrome, Penttinen type776417008
- Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome1172605003
- Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome1172605003
- Laminopathy with premature ageing1177118004
- Laminopathy with premature aging1177118004
- Euthyroid Graves eye disease1197416000
- Euthyroid Graves ophthalmopathy1197416000
- Euthyroid Graves orbitopathy1197416000
- Euthyroid Graves' eye disease1197416000
- Progeroid features, hepatocellular carcinoma predisposition syndrome1216939003
- Ruijs Aalfs syndrome1216939003
- Degeneration of pineal gland1217040009
- Pineal degeneration1217040009
- Pineal gland degeneration1217040009
- Macrogenitosomia praecox due to disorder of pineal gland1217041008
- Macrogenitosomia praecox due to pineal disorder1217041008
- Pellizzi syndrome1217041008
- Macrogenitosomia1217045004
- Calcification of pineal gland1217059006
- Pineal gland calcification1217059006
UMLS
- HGPSC0033300
- HUTCHINSON-GILFORD PROGERIA SYNDROMEC0033300
- Hutchinson Gilford Progeria SyndromeC0033300
- Hutchinson Gilford SyndromeC0033300
- Hutchinson Gilford syndromeC0033300
- Hutchinson-Gilford DiseaseC0033300
- Hutchinson-Gilford Progeria SyndromeC0033300
- Hutchinson-Gilford Progeria SyndromesC0033300
- Hutchinson-Gilford SyndromeC0033300
- Hutchinson-Gilford progeria syndromeC0033300
- Hutchinson-Gilford syndromeC0033300
- Hutchinson-Gilford syndrome (disorder)C0033300
- PROGERIAC0033300
- Premature Senility SyndromeC0033300
- Premature senility syndromeC0033300
- ProgeriaC0033300
- Progeria Syndrome, Hutchinson-GilfordC0033300
- Progeria Syndromes, Hutchinson-GilfordC0033300
- Progeria syndromeC0033300
- hutchinson gilford syndromeC0033300
- hutchinson-gilford syndromeC0033300
- progeriaC0033300
- Other specified endocrine disordersC0029793
- Pineal gland dysfunctionC0271531
- Pineal gland dysfunction (disorder)C0271531
Frequently Asked Questions
What is ICD-10 code E34.8?
ICD-10-CM code E34.8 represents "Other specified endocrine disorders". It 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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.