Chromosomal abnormality, NOS

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ICD10 Diagnosis
Dx: Chromosomal abnormality, NOS
ICD10 code: Q99
Pre-ICD10 counterpart: none assigned
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date:
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • Q99
  • Cargo


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Additional Info

Example: A newborn is discharged with a final diagnosis of uniparental disomy 16. This baby has a number of congenital manifestations: ventricular septal defect (VSD), micrognathia, abnormal elbow, camptodactyly, micropenis, right-sided cryptorchidism and hypospadias. The baby was born at 34 weeks. He also has intrauterine growth restriction (IUGR), weighing 1,200 grams on admission. The baby is discharged after a stay of several weeks.


Other specified chromosome abnormalities/Unspecified intrauterine growth restriction [IUGR]/ low birth weight/Other preterm infants /Ventricular septal defect/Anomaly of jaw size, unspecified/ Other specified congenital musculoskeletal deformities/Congenital deformity of hand/Hypoplasia of penis/Undescended testicle, unilateral/Hypospadias, unspecified/These multiple anomalies are described as due to a chromosomal anomaly

  • Edwards syndrome and Patau syndrome


Chimera 46,XX/46,XY/Chimera 46,XX/46,XY true hermaphrodite/46,XX true hermaphrodite/46,XX with streak gonads/46,XY with streak gonads/Pure gonadal dysgenesis/Fragile X chromosome/Fragile X syndrome

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

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