Malformation/disorder NOS, congenital: Difference between revisions

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'''Includes'''

all such malformations which don't have their own ICD10 codes in our system, which 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/Situs_inversus Situs inversus]

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** [https://en.wikipedia.org/wiki/Alport_syndrome Alport syndrome]

** [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.

*Combine with [[Chromosomal abnormality, NOS]] if appropriate

@@ Line 14: / Line 14: @@
 '''Includes'''
-all such malformations which don't have their own ICD10 codes in our system, which 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/Situs_inversus Situs inversus]
@@ Line 20: / Line 20: @@
 ** [https://en.wikipedia.org/wiki/Alport_syndrome Alport syndrome]
 ** [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.
+*Combine with [[Chromosomal abnormality, NOS]] if appropriate
 {{ICD10 Guideline congenital blindness}}