Malformation/disorder NOS, congenital: Difference between revisions
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== Additional Info == | == Additional Info == | ||
* | '''Includes''' | ||
* all such malformations which don't have their own ICD10 codes in our system, which includes: | |||
** [https://en.wikipedia.org/wiki/Noonan_syndrome Noonan syndrome] | ** [https://en.wikipedia.org/wiki/Noonan_syndrome Noonan syndrome] | ||
** [https://en.wikipedia.org/wiki/Situs_inversus Situs inversus] | ** [https://en.wikipedia.org/wiki/Situs_inversus Situs inversus] | ||
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** [https://en.wikipedia.org/wiki/Alport_syndrome Alport syndrome] | ** [https://en.wikipedia.org/wiki/Alport_syndrome Alport syndrome] | ||
** [https://en.wikipedia.org/wiki/VACTERL_association VACTERL] | ** [https://en.wikipedia.org/wiki/VACTERL_association VACTERL] | ||
**[https://pubmed.ncbi.nlm.nih.gov/21108393/ UBE2A deficiency syndrome] | |||
** Cornelia de Lange syndrome | |||
** Prader-Willi Syndrome combine with [[Chromosomal abnormality, NOS]] | |||
** 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 | |||
{{ICD10 Guideline congenital blindness}} | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||