2008 ICD-9-CM Diagnosis Code 255.2 : Adrenogenital disorders

Free ICD-9-CM Diagnosis Codes > 2008 > Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders 240-279 > Diseases Of Other Endocrine Glands 250-259 > Disorders of adrenal glands 255.* >

2008 ICD-9-CM Diagnosis 255.2

Adrenogenital disorders

255.14

255.3

255.2 is a specific code that can be used to specify a diagnosis on a Medicaid or Medicare reimbursement claim.
Newer versions of 255.2: 2009

Diagnosis Definition(s) Click to expand

Excludes

Also applicable to/known as Click to expand

ICD-9-CM Volume 2 Index Entries That Refer To 255.2 Click to expand

Achard-Thiers syndrome (adrenogenital)

255.2

Adrenocortical syndrome

255.2

Adrenogenital syndrome (acquired) (congenital)

255.2

iatrogenic, fetus or newborn 760.79

Apert-Gallais syndrome (adrenogenital)

255.2

Cooke-Apert-Gallais syndrome (adrenogenital)

255.2

Corticosexual syndrome

255.2

Defect, defective 759.9

3-beta-hydroxysteroid dehydrogenase 255.2
11-hydroxylase 255.2
21-hydroxylase 255.2

Defeminization syndrome

255.2

Deficiency, deficient

3-beta-hydroxysteroid dehydrogenase 255.2
11-beta-hydroxylase 255.2
17-alpha-hydroxylase 255.2
18-hydroxysteroid dehydrogenase 255.2
20-alpha-hydroxylase 255.2
21-hydroxylase 255.2
desmolase 255.2
hydroxylase 255.2

Disorder - see also Disease

adrenogenital 255.2
corticosteroid metabolism NEC 255.2
metabolism NEC 277.9
- corticosteroid 255.2
- steroid 255.2
steroid metabolism NEC 255.2

Hyperadrenocorticism 255.3

congenital 255.2

Hyperfunction

adrenal (cortex) 255.3
- virilism 255.2

Hyperplasia, hyperplastic

adrenal (capsule) (cortex) (gland) 255.8
- with
  - sexual precocity (male) 255.2
  - virilism, adrenal 255.2
  - virilization (female) 255.2
- congenital 255.2

"Infant Hercules" syndrome

255.2

Macrogenitosomia (female) (male) (praecox)

255.2

Masculinization, female, with adrenal hyperplasia

255.2

Precocity, sexual (constitutional) (cryptogenic) (female) (idiopathic) (male) NEC 259.1

with adrenal hyperplasia 255.2

Pseudohermaphroditism 752.7

adrenal 255.2
female (without adrenocortical disorder) 752.7
- with adrenocortical disorder 255.2
- adrenal 255.2
male (without gonadal disorder) 752.7
- with
  - adrenocortical disorder 255.2
- adrenal 255.2

Puberty V21.1

precocious (constitutional) (cryptogenic) (idiopathic) NEC 259.1
- due to
  - adrenal
    - cortical hyperfunction 255.2
    - hyperplasia 255.2
  - cortical hyperfunction 255.2
premature 259.1
- due to
  - adrenal cortical hyperfunction 255.2

Sexual

precocity (constitutional) (cryptogenic) (female) (idiopathic) (male) NEC 259.1
- with adrenal hyperplasia 255.2

Syndrome - see also Disease

Achard-Thiers (adrenogenital) 255.2
adrenogenital (acquired) (congenital) 255.2
- feminizing 255.2
- iatrogenic 760.79
- virilism (acquired) (congenital) 255.2
Apert-Gallais (adrenogenital) 255.2
Cooke-Apert-Gallais (adrenogenital) 255.2
corticosexual 255.2
defeminization 255.2
infant
- Hercules 255.2
pseudohermaphroditism-virilism-hirsutism 255.2
virilizing adrenocortical hyperplasia, congenital 255.2

Virilism (adrenal) (female) NEC

255.2

with
3-beta-hydroxysteroid dehydrogenase defect 255.2
11-hydroxylase defect 255.2
21-hydroxylase defect 255.2
adrenal
- hyperplasia 255.2
- insufficiency (congenital) 255.2
cortical hyperfunction 255.2

Virilization (female) (suprarenal) (see also Virilism)

255.2

isosexual 256.4

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