ICD-10-CM Diagnosis Code Q93.89
Effective Date: 10/01/2015 To 09/30/2025Other deletions from the autosomes
CMS-HCC-V24 | CMS-HCC-V28 | RxHCC | Age | Gender | Maternity | Acute or Chronic | MCC |
---|---|---|---|---|---|---|---|
-- | -- | 148 | -- | -- | -- | Acute | No |
Applicable To for Q93.89:
Back-references to Q93.89
Deletion(s)
Monosomy see also Deletion, chromosome Q93.9
Syndrome see also Disease
- autosome Q93.9
- identified by fluorescence in situ hybridization(FISH) Q93.89
- identified by in situ hybridization(ISH) Q93.89
- identified by fluorescence in situ hybridization(FISH) Q93.89
- chromosome
- seen only at prometaphase Q93.89
- specified NEC Q93.89
- seen only at prometaphase Q93.89
- long arm chromosome 18 or 21 Q93.89
- specified NEC Q93.89
- long arm 18 or 21 deletion Q93.89
Related Medications for
Q93.89
Chapter, Section and Diagnosis Prefix for
Q93.89