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 newborn (P70-P74)
- galactorrhea (N64.3)
- gynecomastia (N62)
- androgen insensitivity syndrome (E34.5-)
- azoospermia or oligospermia NOS (N46.0-N46.1)
- isolated gonadotropin deficiency (E23.0)
- Klinefelter's syndrome (Q98.0-Q98.1, Q98.4)
- postprocedural testicular hypofunction (E89.5)
Use Additional Code
Additional codes that should follow this code
- code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code E29.1?
ICD-10-CM code E29.1 represents "Testicular hypofunction". It 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 you should also code: code for 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.
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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.