Chromosomal abnormality, NOS
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.
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
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