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759.0 ANOMALIES OF SPLEEN


Code Information

Diagnosis Code: 759.0

Short Description: Anomalies of spleen

Long Description: Anomalies of spleen

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 759 Other and unspecified congenital anomalies
        • 759.0 Anomalies of spleen

Code Version: 2015 ICD-9-CM


References to Index of Diseases and Injuries

The code 759.0 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Aberrant (congenital) - see also Malposition, congenital
    • spleen 759.0
  • Absence (organ or part) (complete or partial)
    • spleen (congenital) 759.0
      • acquired V45.79
  • Accessory (congenital)
    • spleen 759.0
  • Agenesis - see also Absence, by site, congenital
    • spleen 759.0
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
    • specified type NEC
      • spleen 759.0
    • spleen 759.0
  • Aplasia - see also Agenesis
    • spleen 759.0
  • Asplenia 759.0
    • with mesocardia 746.87
  • Cyst (mucus) (retention) (serous) (simple)
    • spleen NEC 289.59
      • congenital 759.0
  • Deformity 738.9
    • spleen
      • congenital 759.0
  • Disease, diseased - see also Syndrome
    • polycystic (congenital) 759.89
      • spleen 759.0
    • spleen (organic) (postinfectional) 289.50
      • polycystic 759.0
  • Displacement, displaced
    • spleen, congenital 759.0
  • Distortion (congenital)
    • spleen 759.0
  • Ectopic, ectopia (congenital) 759.89
    • spleen 759.0
  • Enlargement, enlarged - see also Hypertrophy
    • spleen (see also Splenomegaly) 789.2
      • congenital 759.0
  • Hypoplasia, hypoplasis 759.89
    • spleen 759.0
  • Ivemark's syndrome (asplenia with congenital heart disease) 759.0
  • Lobulation (congenital) - see also Anomaly, specified type NEC, by site
    • spleen 759.0
  • Malposition
    • congenital
      • spleen 759.0
  • Paratyphoid (fever) - see Fever, paratyphoid
  • Polycystic (congenital) (disease) 759.89
    • spleen 759.0
  • Polysplenia syndrome 759.0
  • Spleen, splenic - see also condition
    • agenesis 759.0
  • Splenomegaly 789.2
    • congenital 759.0
  • Supernumerary (congenital)
    • spleen 759.0
  • Syndrome - see also Disease
    • Ivemark's (asplenia with congenital heart disease) 759.0
    • polysplenia 759.0
    • splenic
      • agenesis 759.0

Crosswalk Information

The code 759.0 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
759.0 Right Arrow Q89.01 Asplenia (congenital)
Q89.09 Congenital malformations of spleen
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
759.1 Anomalies of adrenal gland
759.2 Anomalies of other endocrine glands
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

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