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Q89.0 - Congenital absence and malformations of spleen


The ICD 10 Code for Congenital absence and malformations of spleen is listed as Q89.0.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field Value
Diagnosis Code: Q89.0
Description: Congenital absence and malformations of spleen
  • Excludes1: isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
Chapter Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Block Other congenital malformations (Q80-Q89)
Parent Q89 - Other congenital malformations, not elsewhere classified
ICD-10-CM Children (deeper level / typically more specific) of Q89.0:
Q89.01 - Asplenia (congenital)
Q89.09 - Congenital malformations of spleen
ICD-10-CM Siblings (same level / similar specificity) of Q89.0:
Q89.1 - Congenital malformations of adrenal gland
Q89.2 - Congenital malformations of other endocrine glands
Q89.3 - Situs inversus
Q89.4 - Conjoined twins
Q89.7 - Multiple congenital malformations, not elsewhere classified
Q89.8 - Other specified congenital malformations
Q89.9 - Congenital malformation, unspecified