E28.39
BillableOther primary ovarian failure
Other primary ovarian failure
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Decreased estrogen
- Resistant ovary syndrome
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(1)
Also Known As / Clinical Terms(228)
SNOMED CT
- Prune belly syndrome5187006
- Triad syndrome5187006
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Female hypogonadism16041008
- Female hypogonadism syndrome16041008
- Congenital absence of abdominal muscle42190000
- Hypogonadism48130008
- Infantilism59892004
- Female hypergonadotropic hypogonadism65846009
- Hypergonadotrophic ovarian failure65846009
- Primary female hypogonadism65846009
- Primary ovarian failure65846009
- Hereditary choroidal atrophy74469006
- Hereditary choroidal dystrophy74469006
- Resistant ovary syndrome80956002
- Corpus luteum deficiency syndrome84304005
- Decreased estrogen level110368006
- Decreased oestrogen level110368006
- Ovarian failure111550004
- Induced female hypogonadism syndrome129633006
- 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
- Incipient ovarian failure237137009
- Menopause ovarian failure237138004
- 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
- POF - Premature ovarian failure237788002
- Premature ovarian failure237788002
- Autoimmune primary ovarian failure237790001
- 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
- Secondary ovarian failure267400004
- Female hypogonadotropic hypogonadism361117008
- Hypergonadotropic hypogonadism370999003
- Primary hypogonadism370999003
- Infantile cataract399120006
- Non age related cataract399305009
- Non age-related cataract399305009
- Nonsenile cataract399305009
- Female infertility due to diminished ovarian reserve427547007
- CACH (childhood ataxia with diffuse central nervous system hypomyelination) syndrome447351004
- Childhood ataxia with diffuse central nervous system hypomyelination447351004
- Leucoencephalopathy with vanishing white matter447351004
- Leukoencephalopathy with vanishing white matter447351004
- Myelinosis centralis diffusa447351004
- Vanishing white matter disease447351004
- 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
- Idiopathic premature ovarian failure721176002
- Premature ovarian failure due to autoimmune oophoritis721198006
- 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
- Osteosclerosis, ichthyosis, premature ovarian failure syndrome722114007
- Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome722114007
- 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
- Ovarioleucodystrophy1156768008
- Ovarioleukodystrophy1156768008
- Fragile X associated primary ovarian insufficiency1332509007
- Female infertility due to ovarian failure217228191000119105
- Infantile and/or juvenile cataract342291000119102
UMLS
- Decreased estrogenC0239302
- Estrogen decreasedC0239302
- Estrogen lowC0239302
- Estrogens decreasedC0239302
- Low estrogenC0239302
- Oestrogen decreasedC0239302
- Oestrogen lowC0239302
- decreased estrogenC0239302
- estrogen lowC0239302
- low estrogenC0239302
- low oestrogenC0239302
- Gonadotropin Resistant Ovary SyndromeC0086367
- Gonadotropin-Resistant Ovary SyndromeC0086367
- Resistant Ovary SyndromeC0086367
- Resistant ovary syndromeC0086367
- Resistant ovary syndrome (disorder)C0086367
- Other primary ovarian failureC2874200
Clinical Terms
- Resistant Ovary Syndrome
- 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
- Progressive cerebellar ataxia
- Female hypergonadotropic hypogonadism
- Female hypogonadism syndrome
- Hypogonadism with mitral valve prolapse and intellectual disability syndrome
- Myelinosis centralis diffusa
- Ovarioleucodystrophy
- Oestrogen decreased
- Female hypogonadotropic hypogonadism
- Premature ovarian failure
- decreased estrogen
- Hypogonadism with prune belly syndrome
- Gonadotropin-Resistant Ovary Syndrome
- low estrogen
- Decreased estrogen level
- Hypogonadal facies
- Secondary ovarian failure
- Truncal obesity
- Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome
- Idiopathic premature ovarian failure
- Leukoencephalopathy with vanishing white matter
- Congenital absence of abdominal muscle
- Infantilism
- Vanishing white matter disease
- Ovarian failure
- Microphthalmia with colobomatous cyst
- Estrogen decreased
- low oestrogen
- Luteinizing hormone-releasing hormone deficiency with ataxia
- Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- Schaap Taylor Baraitser syndrome
- Central obesity
- Childhood ataxia with diffuse central nervous system hypomyelination
- X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome
- Diabetes mellitus associated with genetic syndrome
- Obesity of face and trunk, sparing limbs
- X-linked intellectual disability Ahmad type
- MEHMO syndrome
- Non age related cataract
- Premature ovarian failure due to autoimmune oophoritis
- Primary ovarian failure
- MacDermot Winter syndrome
- Hypogonadal facial wrinkling
- CACH (childhood ataxia with diffuse central nervous system hypomyelination) syndrome
- Female infertility due to ovarian failure
- Ovarioleukodystrophy
- Primary female hypogonadism
- Young Hughes syndrome
- Luteinising hormone-releasing hormone deficiency with ataxia
- Progressive cerebellar ataxia with hypogonadism
- Resistant ovary syndrome (disorder)
- Oestrogen low
- Congenital cataract with deafness and hypogonadism syndrome
- Female infertility due to diminished ovarian reserve
- Fragile X associated primary ovarian insufficiency
- Hypogonadism
- Hydrocephalus with obesity and hypogonadism syndrome
- Prominent glabella with microcephaly and hypogenitalism syndrome
- Bangstad syndrome
- Autoimmune primary ovarian failure
- Corpus luteum deficiency syndrome
- POF - Premature ovarian failure
- Nonsenile cataract
- Cantalamessa Baldini Ambrosi syndrome
- Leucoencephalopathy with vanishing white matter
- Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- Atypical ichthyosis vulgaris with hypogonadism
- Colobomatous microphthalmia
- X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome
- Decreased oestrogen level
- Centripetal obesity
- Primary hypogonadism
- Osteosclerosis, ichthyosis, premature ovarian failure syndrome
- Triad syndrome
- Incipient ovarian failure
- Diabetes, hypogonadism, deafness, intellectual disability syndrome
- Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
- Deafness and hypogonadism syndrome
- Estrogens decreased
- Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
- Hereditary choroidal atrophy
- Prune belly syndrome
- estrogen low
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
- Gonadotropin Resistant Ovary Syndrome
- Boucher Neuhäuser syndrome
- Infantile cataract
- Gordon Holmes syndrome
- Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
- Hypergonadotropic hypogonadism
- Hypergonadotrophic ovarian failure
- Android fat distribution
- Fat body with thin limbs
- Female hypogonadism
- Infantile and/or juvenile cataract
- Microphthalmos co-occurrent with congenital ocular coloboma
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre, and primary gonadal insufficiency
- Hereditary choroidal dystrophy
- Syndromic X-linked intellectual disability type 7
- Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome
- Woodhouse Sakati syndrome
- Retinitis pigmentosa, deafness, mental retardation, hypogonadism syndrome
- Induced female hypogonadism syndrome
- Non age-related cataract
- Menopause ovarian failure
- Sengers Hamel Otten syndrome
Frequently Asked Questions
What is the ICD-10 code for other primary ovarian failure?
The ICD-10-CM code for other primary ovarian failure is E28.39. The full clinical description is "Other primary ovarian failure". E28.39 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E28.39 mean?
ICD-10-CM code E28.39 represents “Other primary ovarian failure”. 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 E28.39 a billable code?
Yes, E28.39 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E28.39 in?
E28.39 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E28.39?
E28.39 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 4 more.
What SNOMED CT codes does E28.39 map to?
E28.39 maps to 55 SNOMED CT concepts: 248311001, 239060009, 237790001, 237614004, 715984007, and 50 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E28.39?
E28.39 is linked to 3 UMLS Concept Unique Identifiers: C0239302, C0086367, C2874200. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E28.39 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other primary ovarian failure 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 E28.39?
There is no direct ICD-11 mapping available for E28.39 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.