Chromosomal abnormality, NOS: Difference between revisions

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*Klinefelter syndrome
*Klinefelter syndrome
*Cri du chat syndrome
*Cri du chat syndrome
* JAK 2 positivity mutation is a frequent genetic event in the three classical Philadelphia-chromosome negative chronic myeloproliferative disorders (Ph(neg.)- CMPD), polycythemia vera (PV), essential thrombocythemia (ET) and idiopathic myelofibrosis (IMF). Its occurrence varies in frequency in regards to phenotype.


'''Examples'''
'''Examples'''

Latest revision as of 07:50, 4 June 2024

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


  • Categories
  • SMW
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories

Additional Info

Includes

  • Anomaly of sex chromosome
  • Autosomal anomaly
  • Chromosomal anomaly
  • Genetic disorder
  • Edwards syndrome and Patau syndrome
  • Chimera 46,XX/46,XY true hermaphrodite
  • 46,XX true hermaphrodite/46,XX with streak gonads
  • 46,XY with streak gonads
  • 46,XY with Pure gonadal dysgenesis
  • Fragile X syndrome
  • 47,XYY
  • Klinefelter syndrome
  • Cri du chat syndrome
  • JAK 2 positivity mutation is a frequent genetic event in the three classical Philadelphia-chromosome negative chronic myeloproliferative disorders (Ph(neg.)- CMPD), polycythemia vera (PV), essential thrombocythemia (ET) and idiopathic myelofibrosis (IMF). Its occurrence varies in frequency in regards to phenotype.

Examples

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Data Integrity Checks (automatic list)

none found

Related Articles

Related articles:


Skin
ENT
Eye

Show all ICD10 Subcategories