Chromosomal abnormality, NOS: Difference between revisions

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{{ICD10 category| Hereditary/congenital}}{{ICD10 category|Misc}}{{ICD10 category|Symptom/Sign}}  
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== Additional Info ==
== 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'''
*Combine this code with [[Ventricular septal defect (VSD), congenital]] if the VSD is due to a chromosomal abnormality
*Anomaly of jaw size, unspecified, combine with [[Disorder of jaws, NOS]]
*Other specified congenital musculoskeletal deformities; These multiple anomalies are described as due to a chromosomal anomaly
**Congenital deformity of hand, combine this code with [[Malformation/disorder NOS, congenital]]
**Hypoplasia of penis combine this code with [[Male genital organs NOS, congenital malformation]]
**Undescended testicle combine this code with [[Male genital organs NOS, congenital malformation]]
**Unilateral/Hypospadias, unspecified combine this code with [[Male genital organs NOS, congenital malformation]]


== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==
(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
* [[Down syndrome (trisomy 21)]]
{sc:Down's, Turner's}
* [[Turner syndrome]]


== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==
(put links to likely candidates coded with this one, eg. a cause for a trauma.)


== Related CCI Codes ==
== Related CCI Codes ==
 
{{Data Integrity Check List}}


== Related Articles ==
== Related Articles ==
{{Related Articles}}
{{Related Articles}}


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{{ICD10 footer}}
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Latest revision as of 08:50, 2024 June 4

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:


Show all ICD10 Subcategories

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