Q89.1
BillableCongenital malformations of adrenal gland
Congenital malformations of adrenal gland
Status
Billable / Specific
Parent Code
Q89Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Accessory adrenal cortex7322007
- Aberrant adrenal gland49494003
- Ectopic adrenal gland49494003
- Congenital anomaly of adrenal gland60637003
- Congenital malformation of adrenal gland60637003
- Accessory adrenal gland68352004
- Supernumerary adrenal gland68352004
- Congenital absence of adrenal gland83190008
- Adrenal rest91285009
- Ectopic adrenal cortex91285009
- Congenital abnormal fusion of adrenal glands92833001
- Congenital fused adrenal glands92833001
- Congenital abnormal shape of adrenal gland92886003
- Congenital misshapen adrenal gland92886003
- Congenital enlarged adrenal gland93068008
- Congenital hypertrophy of adrenal gland93068008
- CAH - Congenital adrenal hypoplasia93235007
- Congenital adrenal hypoplasia93235007
- Congenital hypoplasia of adrenal gland93235007
- Congenital small adrenal gland93235007
- Congenital malposition of adrenal gland93304003
- Congenital malpositioned adrenal gland93304003
- Extracapsular adrenal tissue93452009
- Deficiency of glycerol kinase124322002
- Familial hyperglycerolaemia124322002
- Familial hyperglycerolemia124322002
- GK1 deficiency124322002
- GKD - Glycerol kinase deficiency124322002
- Glycerol kinase deficiency124322002
- Hyperglycerolaemia124322002
- Hyperglycerolemia124322002
- Congenital cyst of adrenal gland205744006
- Enlarged adrenal gland237782001
- Adrenal cyst237784000
- Cyst of adrenal gland237784000
- Disorder of glycerol metabolism237977000
- Abnormal luteotrophic hormone386776005
- Abnormal pituitary interstitial cell stimulating hormone386776005
- Abnormal pituitary luteinising hormone386776005
- Abnormal pituitary luteinizing hormone386776005
- Measurement procedure result absent442228008
- IMAGe syndrome702384004
- Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome702384004
- Adrenal aplasia702615004
- Aplasia of adrenal gland702615004
- SERKAL (sex reversion, kidney, adrenal and lung dysgenesis) syndrome723720008
- SERKAL syndrome723720008
- Sex reversion, kidney, adrenal and lung dysgenesis syndrome723720008
- Familial adrenal hypoplasia miniature type782917007
- Familial adrenal hypoplasia with absent pituitary luteinising hormone782917007
- Familial adrenal hypoplasia with absent pituitary luteinizing hormone782917007
- Hypoplasia of adrenal medulla1144876005
- Adrenal hypertrophy1217058003
- Hypertrophy of adrenal gland1217058003
- MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome1234831009
- MIRAGE syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome1234831009
- Complex GKD (complex glycerol kinase deficiency)1295529002
- Complex glycerol kinase deficiency1295529002
- Xp21 contiguous gene deletion syndrome1295529002
- Xp21 deletion syndrome1295529002
- Xp21 microdeletion syndrome1295529002
- Short stature co-occurrent and due to endocrine disorder368331000119100
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.
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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.