Malformation/disorder NOS, congenital: Difference between revisions
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**[https://pubmed.ncbi.nlm.nih.gov/21108393/ UBE2A deficiency syndrome] | **[https://pubmed.ncbi.nlm.nih.gov/21108393/ UBE2A deficiency syndrome] | ||
** Cornelia de Lange syndrome | ** Cornelia de Lange syndrome | ||
** Prader-Willi 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 | *Combine with [[Chromosomal abnormality, NOS]] if appropriate | ||