AutoICD API

E28.39

Billable

Other primary ovarian failure

Other primary ovarian failure

Status

Billable / Specific

Block

E20-E35

Parent Code

E28.3

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Decreased estrogen
  • Resistant ovary syndrome
Related Codes(1)
Also Known As / Clinical Terms(228)

SNOMED CT

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.