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)
Related Codes(7)
E34.0Carcinoid syndrome
E34.1Other hypersecretion of intestinal hormones
E34.2Ectopic hormone secretion, not elsewhere classified
E34.3Short stature due to endocrine disorder
E34.4Constitutional tall stature
E34.5Androgen insensitivity syndrome
E34.9Endocrine disorder, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(269)
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
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.