Congenital enlarged adrenal gland
Congenital abnormal shape of adrenal gland
CAH - Congenital adrenal hypoplasia
MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome
Abnormal pituitary luteinising hormone
Aplasia of adrenal gland
Hypoplasia of adrenal medulla
Complex GKD (complex glycerol kinase deficiency)
Extracapsular adrenal tissue
Congenital small adrenal gland
Xp21 deletion syndrome
Congenital hypertrophy of adrenal gland
SERKAL (sex reversion, kidney, adrenal and lung dysgenesis) syndrome
Congenital adrenal gland anomaly NOS
Abnormal pituitary luteinizing hormone
Congenital abnormal fusion of adrenal glands
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome
Accessory adrenal gland
Xp21 microdeletion syndrome
Adrenal aplasia
Abnormal luteotrophic hormone
Congenital cyst of adrenal gland
Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome
Glycerol kinase deficiency
Congenital misshapen adrenal gland
Measurement procedure result absent
Adrenal cyst
Familial hyperglycerolaemia
Xp21 contiguous gene deletion syndrome
Accessory adrenal cortex
Congenital anomaly of adrenal gland
Familial adrenal hypoplasia with absent pituitary luteinising hormone
Ectopic adrenal cortex
Hyperglycerolemia
Sex reversion, kidney, adrenal and lung dysgenesis syndrome
Complex glycerol kinase deficiency
Congenital malposition of adrenal gland
Familial adrenal hypoplasia with absent pituitary luteinizing hormone
Congenital hypoplasia of adrenal gland
Ectopic adrenal gland
Congenital malpositioned adrenal gland
Hypertrophy of adrenal gland
IMAGe syndrome
MIRAGE syndrome
Supernumerary adrenal gland
Familial adrenal hypoplasia miniature type
Congenital fused adrenal glands
Disorder of glycerol metabolism
Congenital malformation of adrenal gland
Enlarged adrenal gland
Short stature co-occurrent and due to endocrine disorder
Deficiency of glycerol kinase
GKD - Glycerol kinase deficiency
SERKAL syndrome
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome
GK1 deficiency
Adrenal rest
Familial hyperglycerolemia
Aberrant adrenal gland
Adrenal hypertrophy
Congenital absence of adrenal gland
Cyst of adrenal gland
Hyperglycerolaemia
Congenital anomaly of adrenal gland (disorder)
Abnormal pituitary interstitial cell stimulating hormone
Congenital adrenal hypoplasia
Congenital anomalies of adrenal gland

Frequently Asked Questions

What is the ICD-10 code for congenital malformations of adrenal gland?

The ICD-10-CM code for congenital malformations of adrenal gland is Q89.1. The full clinical description is "Congenital malformations of adrenal gland". Q89.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q89.1 mean?

ICD-10-CM code Q89.1 represents “Congenital malformations of adrenal gland”. 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 Q89.1 a billable code?

Yes, Q89.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q89.1 in?

Q89.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q89.1?

Q89.1 has Excludes1 notes indicating codes that cannot be used together with it, including: adrenogenital disorders (E25.-); congenital adrenal hyperplasia (E25.0).

What SNOMED CT codes does Q89.1 map to?

Q89.1 maps to 28 SNOMED CT concepts: 49494003, 386776005, 7322007, 68352004, 702615004, and 23 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q89.1?

Q89.1 is linked to 1 UMLS Concept Unique Identifier: C0158797. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q89.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformations of adrenal gland 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 Q89.1?

Q89.1 maps to the ICD-11 code: LC8Z (Structural developmental anomalies of the adrenal glands, 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.