Accessory parathyroid gland
Hypophyseal duplication
Congenital hypothyroidism with ectopic thyroid
Duplication of pituitary gland plus syndrome
Bipartite thymus
Congenital absence of parathyroid gland
Cyst, Thyroglossal Duct
thyroglossal duct cysts
Lingual goitre
Endocrine cerebroosteodysplasia syndrome
Accessory thyroid gland
Fetal iodine deficiency syndrome
Congenital anomaly of the thymus
Congenital goitre
Ectopic thyroid tissue
Congenital anomaly of the thyroid gland
Split thymus
Foetal iodine deficiency syndrome
Congenital anomaly of anterior pituitary
Thyroglossal Cyst
Congenital malpositioned thymus
Thyrolingual Cyst
Pharyngeal pituitary tissue
Congenital thymic aplasia
Congenital hypothyroidism without goiter
Thyroxine transport defect
Retinohepatoendocrinologic syndrome
Aplasia of thymus
Congenital anomaly of posterior pituitary
Cysts, Thyrolingual
Congenital malformation of parathyroid gland
Congenital hypothyroidism without goitre
Lingual thyroid
Accessory pituitary gland
cyst duct thyroglossal
Duplication of pituitary gland
ECO syndrome
Congenital malformation of pituitary gland
Cyst, Thyrolingual
Thyrolingual Cysts
Congenital anomaly of endocrine organ
Thyroglossal fistula
Cretinism
thyroglossal duct cyst
Bifid thymus
RHE syndrome
Congenital misshapen thymus
Thyroglossal duct cyst (disorder)
Aberrant pituitary gland
Hypothyroidism sequence
Congenital hypoplasia of anterior pituitary
Autosomal dominant variant form of albumin
Agenesis of parathyroid gland
Congenital malformation of posterior pituitary
Ectopic thymic tissue
Congenital thyroid dystopia
Congenital absence of pituitary gland
Ectopic neurohypophysis
Familial thyroglossal duct cyst
Short stature, pituitary and cerebellar defect and small sella turcica syndrome
Congenital malformation of parathyroid or thyroid gland
Retrosternal thyroid gland
Congenital hypothyroidism not due to iodine deficiency
Ectopic pituitary tissue
Accessory thymic tissue
Anterior pituitary hormone deficiency
Pituitary stalk interruption syndrome
Athyrotic hypothyroidism sequence
Congenital malposition of thymus
Thyrolingual fistula
Congenital goiter
Thymic-renal-anal-lung dysplasia
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland
Congenital anomaly of pituitary gland
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland
Aberrant thyroid gland
Congenital malformation of the endocrine glands
Congenital small thymus
Persistent Thyroglossal Duct
Cone dystrophy
ECO (endocrine-cerebro-osteodysplasia) syndrome
Cervical thyroid remnant
Thymic, renal, anal, lung dysplasia syndrome
Congenital abnormal shape of thymus
Thyroglossal Cysts
Aberrant parathyroid gland
Lingual goiter
Congenital hypoplasia of neurohypophysis
Thyroglossal duct anomaly
Thyroglossal duct sinus
Congenital malposition of the thyroid gland
Familial isolated hypoparathyroidism
Congenital malformation of thymus
Supernumerary thymus
Infantile hypothyroidism
Cysts, Thyroglossal Duct
Cyst, Thyroglossal
Congenital malpositioned thyroid gland
Persistent thyroglossal duct (disorder)
RHE (retinohepatoendocrinologic) syndrome
Congenital cleft of thymus
Congenital anomaly of parathyroid glands
Inherited disorder of thyroid metabolism
Cysts, Thyroglossal
cysts thyroglossal
Congenital hypoplasia of posterior pituitary
Congenital hypothyroidism due to congenital anomaly of thyroid gland
Accessory thymus gland
Agenesis of thymus
Congenital anomaly of endocrine gonad
Aplasia of parathyroid gland
Ectopic parathyroid gland
Congenital absence of thymus
Congenital anomaly of endocrine gland
Congenital hypoplasia of thymus
Aberrant thymus gland
Congenital malformation of anterior pituitary
Sublingual thyroid gland
Endocrine-cerebro-osteodysplasia syndrome
Cervical thymic remnant
Congenital hypoplasia of adenohypophysis
Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome
Congenital iodine deficiency syndrome
Congenital malformation of thyroid gland

Frequently Asked Questions

What is the ICD-10 code for congenital malformations of other endocrine glands?

The ICD-10-CM code for congenital malformations of other endocrine glands is Q89.2. The full clinical description is "Congenital malformations of other endocrine glands". Q89.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q89.2 mean?

ICD-10-CM code Q89.2 represents “Congenital malformations of other endocrine glands”. 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 Q89.2 a billable code?

Yes, Q89.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q89.2 in?

Q89.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q89.2?

Q89.2 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital goiter (E03.0); congenital hypothyroidism (E03.1).

What SNOMED CT codes does Q89.2 map to?

Q89.2 maps to 59 SNOMED CT concepts: 205757003, 6537000, 17422006, 268302006, 65048006, and 54 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q89.2?

Q89.2 is linked to 4 UMLS Concept Unique Identifiers: C2910350, C0432378, C0040124, C0266286. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q89.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformations of other endocrine glands 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 Q89.2?

Q89.2 maps to the ICD-11 code: LD0Z (Structural developmental anomalies primarily affecting one body system, 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.