E29.1
BillableTesticular hypofunction
Testicular hypofunction
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Defective biosynthesis of testicular androgen NOS
- 5-delta-Reductase deficiency (with male pseudohermaphroditism)
- Testicular hypogonadism NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •galactorrheaN64.3
- •gynecomastiaN62
- •androgen insensitivity syndromeE34.5
- •azoospermia or oligospermia NOSN46.0-N46.1
- •isolated gonadotropin deficiencyE23.0
- •Klinefelter's syndrome,Q98.0-Q98.1, Q98.4
- •postprocedural testicular hypofunctionE89.5
Use Additional Code
Additional codes that should follow this code
Related Codes(3)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(246)
SNOMED CT
- Prune belly syndrome5187006
- Triad syndrome5187006
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Androgen receptor abnormal9979004
- Disorder of androgen receptor9979004
- Androgen deficiency38825009
- Defect of testicular androgen synthesis38825009
- Defective biosynthesis of testicular androgen38825009
- Deficiency of testosterone biosynthesis38825009
- Congenital absence of abdominal muscle42190000
- Hypogonadism48130008
- Eunuchoidism48723006
- Eunuchoidism hypogonadism48723006
- Eunuchoidism, hypogonadism48723006
- Male hypogonadism48723006
- Primary gonadal failure48723006
- Primary male hypogonadism48723006
- Testicular failure48723006
- Testicular hypogonadism48723006
- Infantilism59892004
- Seminiferous tubule failure in adult60607007
- Hereditary choroidal atrophy74469006
- Hereditary choroidal dystrophy74469006
- Leydig cell failure in adult82560004
- Testicular hypofunction111551000
- Induced male hypogonadism syndrome129634000
- Progressive cerebellar ataxia230233000
- Gordon Holmes syndrome230240004
- Luteinising hormone-releasing hormone deficiency with ataxia230240004
- Luteinizing hormone-releasing hormone deficiency with ataxia230240004
- Progressive cerebellar ataxia with hypogonadism230240004
- Hypogonadism with prune belly syndrome236796004
- Acquired male infertility236809006
- Acquired testicular failure236811002
- Bangstad syndrome237614004
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency237614004
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency237614004
- Undervirilisation237807003
- Undervirilization237807003
- Cutaneous syndrome with ichthyosis239057002
- Atypical ichthyosis vulgaris with hypogonadism239060009
- Hypogonadal facies248203009
- Hypogonadal facial wrinkling248204003
- Android fat distribution248311001
- Central obesity248311001
- Centripetal obesity248311001
- Fat body with thin limbs248311001
- Obesity of face and trunk, sparing limbs248311001
- Truncal obesity248311001
- Defective synthesis of 17B hydroxysteroid dehydrogenase267402007
- Testicular hypofunction due to defect in adrenocortical hormone synthesis267402007
- Eunuchism267403002
- Primary failure of the testes370997001
- Primary testicular failure370997001
- Hypergonadotropic hypogonadism370999003
- Primary hypogonadism370999003
- Infantile cataract399120006
- Non age related cataract399305009
- Non age-related cataract399305009
- Nonsenile cataract399305009
- Undervirilisation of male due to steroidogenic acute regulatory protein deficiency444173008
- Undervirilization of male due to steroidogenic acute regulatory protein deficiency444173008
- Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome715429006
- Colobomatous microphthalmia715771008
- Microphthalmia with colobomatous cyst715771008
- Microphthalmos co-occurrent with congenital ocular coloboma715771008
- Boucher Neuhäuser syndrome715984007
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome715984007
- MacDermot Winter syndrome716023007
- Prominent glabella with microcephaly and hypogenitalism syndrome716023007
- Deafness and hypogonadism syndrome718714006
- Syndromic X-linked intellectual disability type 7719160009
- X-linked intellectual disability Ahmad type719160009
- Hydrocephalus with obesity and hypogonadism syndrome721231007
- Sengers Hamel Otten syndrome721231007
- Cantalamessa Baldini Ambrosi syndrome721841001
- Hypogonadism with mitral valve prolapse and intellectual disability syndrome721841001
- Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome722037004
- MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) syndrome722037004
- MEHMO syndrome722037004
- Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome722037004
- X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome722037004
- Congenital cataract with deafness and hypogonadism syndrome722378009
- Schaap Taylor Baraitser syndrome722378009
- Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome722454003
- Mental retardation syndrome Belgian type722454003
- Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome724001005
- Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome724001005
- X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome765471005
- Young Hughes syndrome765471005
- Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome776204008
- Diabetes, hypogonadism, deafness, intellectual disability syndrome816067005
- Woodhouse Sakati syndrome816067005
- Testicular hypofunction caused by ionising radiation1338060006
- Testicular hypofunction caused by ionizing radiation1338060006
- Infantile and/or juvenile cataract342291000119102
UMLS
- 5-delta-Reductase deficiency (with male pseudohermaphroditism)C2874201
- Androgen deficiencyC0342527
- Androgen insufficiencyC0342527
- Defect of testicular androgen synthesisC0342527
- Defective biosynthesis of testicular androgenC0342527
- Defective biosynthesis of testicular androgen NOSC0342527
- Deficiency of testosterone biosynthesisC0342527
- Deficiency of testosterone biosynthesis (disorder)C0342527
- HypoandrogenismC0342527
- Testosterone Biosynthesis DeficiencyC0342527
- androgen deficiencyC0342527
- Decreased function of male gonadC0151721
- EunuchoidismC0151721
- Eunuchoidism hypogonadismC0151721
- Eunuchoidism, hypogonadismC0151721
- HYPOGONADISM, MALEC0151721
- Hypogonadism (in males)C0151721
- Hypogonadism maleC0151721
- Hypogonadism, MaleC0151721
- Male hypogonadismC0151721
- Male hypogonadism (disorder)C0151721
- Testicular FailureC0151721
- Testicular failureC0151721
- Testicular failure NOSC0151721
- Testicular hypogonadismC0151721
- Testicular hypogonadism NOSC0151721
- eunuchoidismC0151721
- failure testicularC0151721
- hypogonadism maleC0151721
- hypogonadism malesC0151721
- male hypogonadismC0151721
- testicular failureC0151721
- Hypofunction testicleC0271622
- Testicular hypofunctionC0271622
- Testicular hypofunction (disorder)C0271622
- testicular hypofunctionC0271622
Clinical Terms
- Mental retardation syndrome Belgian type
- Cutaneous syndrome with ichthyosis
- Genetic syndromes of diabetes mellitus
- MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) syndrome
- Defective biosynthesis of testicular androgen NOS
- Progressive cerebellar ataxia
- Hypogonadism with mitral valve prolapse and intellectual disability syndrome
- Primary gonadal failure
- Testicular failure
- Deficiency of testosterone biosynthesis (disorder)
- Hypogonadism with prune belly syndrome
- Androgen deficiency
- Acquired male infertility
- Primary male hypogonadism
- Hypogonadal facies
- Truncal obesity
- Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome
- Eunuchism
- Congenital absence of abdominal muscle
- Undervirilisation
- Infantilism
- Microphthalmia with colobomatous cyst
- Primary failure of the testes
- Luteinizing hormone-releasing hormone deficiency with ataxia
- Seminiferous tubule failure in adult
- Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- Schaap Taylor Baraitser syndrome
- Central obesity
- X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
- Diabetes mellitus associated with genetic syndrome
- 5-delta-Reductase deficiency (with male pseudohermaphroditism)
- Obesity of face and trunk, sparing limbs
- X-linked intellectual disability Ahmad type
- MEHMO syndrome
- Non age related cataract
- Hypofunction testicle
- Hypogonadism male
- MacDermot Winter syndrome
- Hypogonadal facial wrinkling
- Undervirilisation of male due to steroidogenic acute regulatory protein deficiency
- Testicular hypogonadism NOS
- Eunuchoidism hypogonadism
- Hypoandrogenism
- Eunuchoidism
- Young Hughes syndrome
- Defective synthesis of 17B hydroxysteroid dehydrogenase
- Eunuchoidism, hypogonadism
- Luteinising hormone-releasing hormone deficiency with ataxia
- Defective biosynthesis of testicular androgen
- Progressive cerebellar ataxia with hypogonadism
- Leydig cell failure in adult
- Congenital cataract with deafness and hypogonadism syndrome
- Defect of testicular androgen synthesis
- Testicular failure NOS
- Hypogonadism (in males)
- Hypogonadism
- Undervirilization of male due to steroidogenic acute regulatory protein deficiency
- Testicular hypofunction (disorder)
- Hydrocephalus with obesity and hypogonadism syndrome
- Prominent glabella with microcephaly and hypogenitalism syndrome
- Deficiency of testosterone biosynthesis
- Androgen insufficiency
- Bangstad syndrome
- Hypogonadism, Male
- Undervirilization
- Nonsenile cataract
- failure testicular
- Cantalamessa Baldini Ambrosi syndrome
- Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- Induced male hypogonadism syndrome
- Atypical ichthyosis vulgaris with hypogonadism
- Colobomatous microphthalmia
- Testicular hypofunction caused by ionising radiation
- X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
- Centripetal obesity
- Primary hypogonadism
- Triad syndrome
- Diabetes, hypogonadism, deafness, intellectual disability syndrome
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
- Deafness and hypogonadism syndrome
- Primary testicular failure
- Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
- Male hypogonadism (disorder)
- Hereditary choroidal atrophy
- Prune belly syndrome
- Testicular hypofunction caused by ionizing radiation
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
- Boucher Neuhäuser syndrome
- Infantile cataract
- Gordon Holmes syndrome
- Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
- Hypergonadotropic hypogonadism
- Testicular hypofunction due to defect in adrenocortical hormone synthesis
- Android fat distribution
- Acquired testicular failure
- Fat body with thin limbs
- Androgen receptor abnormal
- Testicular hypogonadism
- Male hypogonadism
- Infantile and/or juvenile cataract
- Microphthalmos co-occurrent with congenital ocular coloboma
- Disorder of androgen receptor
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency
- Hereditary choroidal dystrophy
- Syndromic X-linked intellectual disability type 7
- Decreased function of male gonad
- hypogonadism males
- Testosterone Biosynthesis Deficiency
- Woodhouse Sakati syndrome
- Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome
- Non age-related cataract
- Sengers Hamel Otten syndrome
Frequently Asked Questions
What is the ICD-10 code for testicular hypofunction?
The ICD-10-CM code for testicular hypofunction is E29.1. The full clinical description is "Testicular hypofunction". E29.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E29.1 mean?
ICD-10-CM code E29.1 represents “Testicular hypofunction”. 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 E29.1 a billable code?
Yes, E29.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E29.1 in?
E29.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E29.1?
E29.1 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 5 more.
Are additional codes required with E29.1?
Yes, when using E29.1, also report: adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5).
What SNOMED CT codes does E29.1 map to?
E29.1 maps to 49 SNOMED CT concepts: 236809006, 236811002, 38825009, 9979004, 248311001, and 44 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E29.1?
E29.1 is linked to 4 UMLS Concept Unique Identifiers: C2874201, C0342527, C0151721, C0271622. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E29.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like testicular hypofunction 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 E29.1?
E29.1 maps to the ICD-11 code: 5A81.1 (Testicular hypofunction).
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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.