759.2 ENDOCRINE ANOMALY NEC


Code Information

Diagnosis Code: 759.2

Short Description: Endocrine anomaly NEC

Long Description: Anomalies of other endocrine glands

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 759 Other and unspecified congenital anomalies
        • 759.2 Endocrine anomaly NEC

Code Version: 2015 ICD-9-CM


Synonyms

  • Aberrant parathyroid gland
  • Aberrant thyroid gland
  • Absence of hormonal activity
  • Absent parathyroid gland
  • Accessory parathyroid gland
  • Accessory pituitary gland
  • Accessory thymic tissue
  • Accessory thyroid gland
  • Aplasia of parathyroid gland
  • Aplasia of thymus
  • Cervical thymic remnant
  • Cervical thyroid remnant
  • Congenital abnormal shape of thymus
  • Congenital absence of parathyroid gland
  • Congenital absence of pituitary gland
  • Congenital absence of thymus
  • Congenital absence of thyroid gland
  • 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 hypothyroidism with ectopic thyroid
  • Congenital malformation of anterior pituitary
  • Congenital malformation of posterior pituitary
  • Congenital malposition of the thyroid gland
  • Congenital malposition of thymus
  • Ectopic pituitary tissue
  • Ectopic thymic tissue
  • Ectopic thyroid tissue
  • Female Kallman's syndrome
  • General loss of peroxisomal function
  • Lingual goiter
  • Lingual thyroid
  • Persistent thyroglossal duct
  • Pharyngeal pituitary tissue
  • Retrosternal thyroid gland
  • Thyroglossal duct anomaly
  • Thyroglossal duct cyst
  • Thyroglossal duct sinus

References to Index of Diseases and Injuries

The code 759.2 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Aberrant (congenital) - see also Malposition, congenital
    • endocrine gland NEC 759.2
    • parathyroid gland 759.2
    • pituitary gland (pharyngeal) 759.2
    • thymus gland 759.2
    • thyroid gland 759.2
  • Absence (organ or part) (complete or partial)
    • endocrine gland NEC (congenital) 759.2
    • parathyroid gland (congenital) 759.2
    • pituitary gland (congenital) 759.2
    • thymus gland (congenital) 759.2
  • Accessory (congenital)
    • endocrine gland NEC 759.2
    • parathyroid gland 759.2
    • pituitary gland 759.2
    • thymus gland 759.2
    • thyroid gland 759.2
  • Agenesis - see also Absence, by site, congenital
    • endocrine (gland) NEC 759.2
    • parathyroid (gland) 759.2
    • pituitary (gland) 759.2
    • thymus (gland) 759.2
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
    • endocrine gland NEC 759.2
    • hypophyseal 759.2
    • parathyroid gland 759.2
    • pituitary (gland) 759.2
    • specified type NEC
      • endocrine 759.2
      • parathyroid 759.2
      • pituitary 759.2
      • thymus 759.2
      • thyroid (gland) 759.2
        • cartilage 748.3
    • thymus gland 759.2
    • thyroid (gland) 759.2
      • cartilage 748.3
  • Cyst (mucus) (retention) (serous) (simple)
    • congenital NEC 759.89
      • thymus (gland) 759.2
    • thyroglossal (duct) (infected) (persistent) 759.2
    • thyrolingual duct (infected) (persistent) 759.2
  • Deformity 738.9
    • endocrine gland NEC 759.2
    • hypophyseal (congenital) 759.2
    • parathyroid (gland) 759.2
    • pituitary (congenital) 759.2
    • thymus (tissue) (congenital) 759.2
    • thyroid (gland) (congenital) 759.2
      • cartilage 748.3
        • acquired 478.79
  • Distortion (congenital)
    • endocrine (gland) NEC 759.2
    • parathyroid (gland) 759.2
    • pituitary (gland) 759.2
    • thymus (gland) 759.2
    • thyroid (gland) 759.2
      • cartilage 748.3
  • Ectopic, ectopia (congenital) 759.89
    • thyroid 759.2
  • Fistula (sinus) 686.9
    • thyroglossal duct 759.2
  • Goiter (adolescent) (colloid) (diffuse) (dipping) (due to iodine deficiency) (endemic) (euthyroid) (heart) (hyperplastic) (internal) (intrathoracic) (juvenile) (mixed type) (nonendemic) (parenchymatous) (plunging) (sporadic) (subclavicular) (substernal) 240.9
    • lingual 759.2
  • Hypoplasia, hypoplasis 759.89
    • endocrine (gland) NEC 759.2
    • parathyroid (gland) 759.2
    • pituitary (gland) 759.2
  • Lingual (tongue) - see also condition
    • thyroid 759.2
  • Malposition
    • congenital
      • endocrine (gland) NEC 759.2
      • parathyroid (gland) 759.2
      • pituitary (gland) 759.2
      • thymus (gland) 759.2
      • thyroid (gland) (tissue) 759.2
        • cartilage 748.3
  • Nasopharyngeal - see also condition
    • pituitary gland 759.2
  • Paratyphoid (fever) - see Fever, paratyphoid
  • Persistence, persistent (congenital) 759.89
    • thyroglossal duct 759.2
    • thyrolingual duct 759.2
  • Remnant
    • thyroglossal duct 759.2
  • Retrosternal thyroid (congenital) 759.2
  • Substernal thyroid (see also Goiter) 240.9
    • congenital 759.2
  • Thyroglossal - see also condition
    • cyst 759.2
    • duct, persistent 759.2
  • Thyroid (body) (gland) - see also condition
    • lingual 759.2
  • Thyrolingual duct, persistent 759.2

Crosswalk Information

The code 759.2 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
759.2 Right Arrow Q89.2 Congenital malformations of other endocrine glands
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
759.0 Anomalies of spleen
759.1 Anomalies of adrenal gland
759.3 Situs inversus
759.4 Conjoined twins
759.5 Tuberous sclerosis
759.6 Other hamartoses, not elsewhere classified
759.7 Multiple congenital anomalies, so described
759.81 Prader-Willi syndrome
759.82 Marfan syndrome
759.83 Fragile X syndrome
759.89 Other specified congenital anomalies
759.9 Congenital anomaly, unspecified


This page was last updated on: 10/1/2014