Malformation/disorder NOS, congenital: Difference between revisions

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** Cornelia de Lange syndrome
** Cornelia de Lange syndrome
** Prader-Willi Syndrome
** Prader-Willi Syndrome
** Birt Hogg Dube Syndrome
*If a patient has both a malformation for which our system has a specific code (e.g. [[Down syndrome (trisomy 21)|Down syndrome]]) and one or more malformations which fit here, then list both.
*If a patient has both a malformation for which our system has a specific code (e.g. [[Down syndrome (trisomy 21)|Down syndrome]]) and one or more malformations which fit here, then list both.
*Combine with [[Chromosomal abnormality, NOS]] if appropriate
*Combine with [[Chromosomal abnormality, NOS]] if appropriate

Latest revision as of 08:48, 2024 March 12

ICD10 Diagnosis
Dx: Malformation/disorder NOS, congenital
ICD10 code: Q89
Pre-ICD10 counterpart: Noonan syndrome
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
    • Q89
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories
  • SMW
  • Cargo


  • Categories

Additional Info

Includes


Congenital Blindness

Congenital blindness can occur due to actual eye problems or due to problems with the visual nerves or brain. Thus, for this relatively rare entity, code Combined ICD10 codes of Blindness, both eyes (or if appropriate Blindness, one eye) and Malformation/disorder NOS, congenital.

Alternate ICD10s to consider coding instead or in addition

Candidate Combined ICD10 codes

Related CCI Codes

Data Integrity Checks (automatic list)

none found

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