Q56.2
BillableFemale pseudohermaphroditism, not elsewhere classified
Female pseudohermaphroditism, not elsewhere classified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Female pseudohermaphroditism NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •androgen insensitivity syndromeE34.5
- •syndromes associated with anomalies in the number and form of chromosomesQ90-Q99
- •46,XX true hermaphroditeQ99.1
- •chimera 46,XX/46,XY true hermaphroditeQ99.0
- •female pseudohermaphroditism with adrenocortical disorderE25
- •pseudohermaphroditism with specified chromosomal anomalyQ96-Q99
- •pure gonadal dysgenesisQ99.1
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(55)
SNOMED CT
- Female pseudohermaphroditism8800006
- Ferms8800006
- Gynandrism8800006
- Ambiguous genitalia21321009
- Anal atresia204712000
- Aproctia204712000
- Atresia ani204712000
- Congenital atresia of anus204712000
- Congenital imperforate anus204712000
- Imperforate anus204712000
- 46,XX disorder of sex development with skeletal anomalies syndrome733621007
- Female pseudohermaphroditism with skeletal anomalies syndrome733621007
- 46,XX disorder of sex development with anorectal anomalies syndrome733622000
- Female pseudohermaphroditism with anorectal anomalies syndrome733622000
- 46,XX disorder of sex development due to maternal Krukenberg neoplasm838326005
- 46,XX disorder of sex development due to maternal arrhenoblastoma838327001
- 46,XX disorder of sex development due to maternal androluteoma838328006
- 46,XX disorder of sex development due to maternal adrenal neoplasm838329003
UMLS
- Female PseudohermaphroditismC0238394
- Female PseudohermaphroditismsC0238394
- Female pseudohermaphroditismC0238394
- Female pseudohermaphroditism (disorder)C0238394
- Female pseudohermaphroditism NOSC0238394
- FermsC0238394
- GynandrismC0238394
- Pseudohermaphroditism femaleC0238394
- Pseudohermaphroditism, FemaleC0238394
- Pseudohermaphroditisms, FemaleC0238394
- female pseudohermaphroditismC0238394
- fermC0238394
- Female pseudohermaphroditism, not elsewhere classifiedC0495579
Clinical Terms
- ferm
- Female pseudohermaphroditism with anorectal anomalies syndrome
- Female Pseudohermaphroditisms
- 46,XX disorder of sex development due to maternal androluteoma
- 46,XX disorder of sex development due to maternal Krukenberg neoplasm
- Ambiguous genitalia
- Gynandrism
- 46,XX disorder of sex development with skeletal anomalies syndrome
- Imperforate anus
- 46,XX disorder of sex development with anorectal anomalies syndrome
- Female pseudohermaphroditism NOS
- Female pseudohermaphroditism (disorder)
- Atresia ani
- 46,XX disorder of sex development due to maternal arrhenoblastoma
- Ferms
- 46,XX disorder of sex development due to maternal adrenal neoplasm
- Aproctia
- Anal atresia
- Pseudohermaphroditism female
- Pseudohermaphroditisms, Female
- Congenital atresia of anus
- Female pseudohermaphroditism with skeletal anomalies syndrome
- Pseudohermaphroditism, Female
- Congenital imperforate anus
Frequently Asked Questions
What is the ICD-10 code for female pseudohermaphroditism, not elsewhere classified?
The ICD-10-CM code for female pseudohermaphroditism, not elsewhere classified is Q56.2. The full clinical description is "Female pseudohermaphroditism, not elsewhere classified". Q56.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q56.2 mean?
ICD-10-CM code Q56.2 represents “Female pseudohermaphroditism, not elsewhere classified”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q56.2 a billable code?
Yes, Q56.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q56.2 in?
Q56.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q56.2?
Q56.2 has Excludes1 notes indicating codes that cannot be used together with it, including: androgen insensitivity syndrome (E34.5-); syndromes associated with anomalies in the number and form of chromosomes (Q90-Q99); 46,XX true hermaphrodite (Q99.1); and 4 more.
What SNOMED CT codes does Q56.2 map to?
Q56.2 maps to 9 SNOMED CT concepts: 838326005, 838329003, 838328006, 838327001, 733622000, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q56.2?
Q56.2 is linked to 2 UMLS Concept Unique Identifiers: C0238394, C0495579. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q56.2 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like female pseudohermaphroditism, not elsewhere classified 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 Q56.2?
Q56.2 maps to the ICD-11 code: LD2A.Z (Malformative disorders of sex development, unspecified).
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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.