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)
Also Known As / Clinical Terms
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
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.
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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.