Present on admission (POA) is defined as present at the time the order for inpatient admission occurs - conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered as present on admission.
See the POA Reporting Guidelines for more information.
| Code | Description |
|---|---|
| Q86.1 | Fetal hydantoin syndrome |
| Q86.1 | Fetal hydantoin syndrome |
| Q86.1 | Fetal hydantoin syndrome |
| Q86.2 | Dysmorphism due to warfarin |
| Q86.2 | Dysmorphism due to warfarin |
| Q86.2 | Dysmorphism due to warfarin |
| Q86.2 | Dysmorphism due to warfarin |
| Q86.8 | Other congenital malformation syndromes due to known exogenous causes |
| Q86.8 | Other congenital malformation syndromes due to known exogenous causes |
| Q86.8 | Other congenital malformation syndromes due to known exogenous causes |
| Q86.8 | Other congenital malformation syndromes due to known exogenous causes |
| Q87.0 | Congenital malformation syndromes predominantly affecting facial appearance |
| Q87.0 | Congenital malformation syndromes predominantly affecting facial appearance |
| Q87.0 | Congenital malformation syndromes predominantly affecting facial appearance |
| Q87.0 | Congenital malformation syndromes predominantly affecting facial appearance |
| Q87.11 | Prader-Willi syndrome |
| Q87.11 | Prader-Willi syndrome |
| Q87.11 | Prader-Willi syndrome |
| Q87.11 | Prader-Willi syndrome |
| Q87.19 | Other congenital malformation syndromes predominantly associated with short stature |
| Q87.19 | Other congenital malformation syndromes predominantly associated with short stature |
| Q87.19 | Other congenital malformation syndromes predominantly associated with short stature |
| Q87.19 | Other congenital malformation syndromes predominantly associated with short stature |
| Q87.2 | Congenital malformation syndromes predominantly involving limbs |
| Q87.2 | Congenital malformation syndromes predominantly involving limbs |
| Q87.2 | Congenital malformation syndromes predominantly involving limbs |
| Q87.2 | Congenital malformation syndromes predominantly involving limbs |
| Q87.3 | Congenital malformation syndromes involving early overgrowth |
| Q87.3 | Congenital malformation syndromes involving early overgrowth |
| Q87.3 | Congenital malformation syndromes involving early overgrowth |
| Q87.3 | Congenital malformation syndromes involving early overgrowth |
| Q87.40 | Marfan syndrome, unspecified |
| Q87.40 | Marfan syndrome, unspecified |
| Q87.40 | Marfan syndrome, unspecified |
| Q87.40 | Marfan syndrome, unspecified |
| Q87.410 | Marfan syndrome with aortic dilation |
| Q87.410 | Marfan syndrome with aortic dilation |
| Q87.410 | Marfan syndrome with aortic dilation |
| Q87.410 | Marfan syndrome with aortic dilation |
| Q87.418 | Marfan syndrome with other cardiovascular manifestations |
| Q87.418 | Marfan syndrome with other cardiovascular manifestations |
| Q87.418 | Marfan syndrome with other cardiovascular manifestations |
| Q87.418 | Marfan syndrome with other cardiovascular manifestations |
| Q87.42 | Marfan syndrome with ocular manifestations |
| Q87.42 | Marfan syndrome with ocular manifestations |
| Q87.42 | Marfan syndrome with ocular manifestations |
| Q87.42 | Marfan syndrome with ocular manifestations |
| Q87.43 | Marfan syndrome with skeletal manifestation |
| Q87.43 | Marfan syndrome with skeletal manifestation |
| Q87.43 | Marfan syndrome with skeletal manifestation |