Diagnosis Code: Q89.2

Short Description: Congenital malformations of other endocrine glands

Long Description: Congenital malformations of other endocrine glands

The code Q89.2 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Other congenital malformations, not elsewhere classified (Q89)
      • Q89.2 Congenital malformations of other endocrine glands

Code Version: 2022 ICD-10-CM

Synonyms

• Aberrant parathyroid gland
• Aberrant thyroid gland
• Accessory parathyroid gland
• Accessory pituitary gland
• Accessory thymic tissue
• Accessory thyroid gland
• Agenesis of thymus
• Anterior pituitary hormone deficiency
• Aplasia of parathyroid gland
• Aplasia of thymus
• Athyrotic hypothyroidism sequence
• Autosomal dominant variant form of albumin
• Cervical thymic remnant
• Cervical thyroid remnant
• Cone dystrophy
• Congenital abnormal shape of thymus
• Congenital absence of parathyroid gland
• Congenital absence of pituitary gland
• Congenital absence of thymus
• Congenital anomaly of endocrine gland
• Congenital anomaly of endocrine gonad
• Congenital anomaly of parathyroid glands
• Congenital anomaly of pituitary gland
• Congenital anomaly of the thymus
• Congenital anomaly of the thyroid gland
• Congenital cleft of thymus
• Congenital hypoplasia of cerebrum
• Congenital hypoplasia of thymus
• Congenital hypothyroidism due to congenital anomaly of thyroid gland
• Congenital hypothyroidism with ectopic thyroid
• Congenital hypothyroidism without goiter
• Congenital iodine deficiency syndrome
• Congenital malformation of anterior pituitary
• Congenital malformation of anterior pituitary
• Congenital malformation of posterior pituitary
• Congenital malposition of the thyroid gland
• Congenital malposition of thymus
• Duplication of pituitary gland
• Ectopic pituitary tissue
• Ectopic pituitary tissue
• Ectopic thymic tissue
• Endocrine-cerebro-osteodysplasia syndrome
• Familial thyroglossal duct cyst
• Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland
• Inherited disorder of thyroid metabolism
• Lingual goiter
• Lingual thyroid
• Persistent thyroglossal duct
• Pharyngeal pituitary tissue
• Pituitary stalk interruption syndrome
• Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome
• Retinohepatoendocrinologic syndrome
• Retrosternal thyroid gland
• Short stature, pituitary and cerebellar defect and small sella turcica syndrome
• Thymic, renal, anal, lung dysplasia syndrome
• Thyroglossal duct anomaly
• Thyroglossal duct cyst
• Thyroglossal duct sinus
• Thyroxine transport defect

Diagnostic Related Group(s)

The code Q89.2 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Endocrine Disorders With Mcc (643)
• Endocrine Disorders With Cc (644)
• Endocrine Disorders Without Cc/mcc (645)

References to Index of Diseases and Injuries

The code Q89.2 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital malformation of parathyroid or thyroid gland
  • Persistent thyroglossal duct
  • Thyroglossal cyst
• Type 1 Excludes Notes:
  • congenital goiter (@E03.0*)
  • congenital hypothyroidism (@E03.1*)

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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