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3. Present On Admission Exempt ICD-10-CM Codes

Present On Admission Exempt ICD-10-CM Codes

Present On Admission 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 POA. The following 37,658 ICD-10-CM codes are considered exempt from POA reporting.

Displaying codes 401-500 of 37,658:

• P00.81
  Newborn affected by periodontal disease in mother
• P00.82
  Newborn affected by (positive) maternal group B streptococcus (GBS) colonization
• P00.89
  Newborn affected by other maternal conditions
• P00.9
  Newborn affected by unspecified maternal condition
• P29.30
  Pulmonary hypertension of newborn
• P29.38
  Other persistent fetal circulation
• P78.84
  Gestational alloimmune liver disease
• P83.81
  Umbilical granuloma
• P83.88
  Other specified conditions of integument specific to newborn
• P91.811
  Neonatal encephalopathy in diseases classified elsewhere
• P91.819
  Neonatal encephalopathy, unspecified
• P91.821
  Neonatal cerebral infarction, right side of brain
• P91.822
  Neonatal cerebral infarction, left side of brain
• P91.823
  Neonatal cerebral infarction, bilateral
• P91.829
  Neonatal cerebral infarction, unspecified side
• P91.88
  Other specified disturbances of cerebral status of newborn
• Q00.0
  Anencephaly
• Q00.1
  Craniorachischisis
• Q00.2
  Iniencephaly
• Q01.0
  Frontal encephalocele
• Q01.1
  Nasofrontal encephalocele
• Q01.2
  Occipital encephalocele
• Q01.8
  Encephalocele of other sites
• Q01.9
  Encephalocele, unspecified
• Q02
  Microcephaly
• Q03.0
  Malformations of aqueduct of Sylvius
• Q03.1
  Atresia of foramina of Magendie and Luschka
• Q03.8
  Other congenital hydrocephalus
• Q03.9
  Congenital hydrocephalus, unspecified
• Q04.0
  Congenital malformations of corpus callosum
• Q04.1
  Arhinencephaly
• Q04.2
  Holoprosencephaly
• Q04.3
  Other reduction deformities of brain
• Q04.4
  Septo-optic dysplasia of brain
• Q04.5
  Megalencephaly
• Q04.6
  Congenital cerebral cysts
• Q04.8
  Other specified congenital malformations of brain
• Q04.9
  Congenital malformation of brain, unspecified
• Q05.0
  Cervical spina bifida with hydrocephalus
• Q05.1
  Thoracic spina bifida with hydrocephalus
• Q05.2
  Lumbar spina bifida with hydrocephalus
• Q05.3
  Sacral spina bifida with hydrocephalus
• Q05.4
  Unspecified spina bifida with hydrocephalus
• Q05.5
  Cervical spina bifida without hydrocephalus
• Q05.6
  Thoracic spina bifida without hydrocephalus
• Q05.7
  Lumbar spina bifida without hydrocephalus
• Q05.8
  Sacral spina bifida without hydrocephalus
• Q05.9
  Spina bifida, unspecified
• Q06.0
  Amyelia
• Q06.1
  Hypoplasia and dysplasia of spinal cord
• Q06.2
  Diastematomyelia
• Q06.3
  Other congenital cauda equina malformations
• Q06.4
  Hydromyelia
• Q06.8
  Other specified congenital malformations of spinal cord
• Q06.9
  Congenital malformation of spinal cord, unspecified
• Q07.00
  Arnold-Chiari syndrome without spina bifida or hydrocephalus
• Q07.01
  Arnold-Chiari syndrome with spina bifida
• Q07.02
  Arnold-Chiari syndrome with hydrocephalus
• Q07.03
  Arnold-Chiari syndrome with spina bifida and hydrocephalus
• Q07.8
  Other specified congenital malformations of nervous system
• Q07.9
  Congenital malformation of nervous system, unspecified
• Q10.0
  Congenital ptosis
• Q10.1
  Congenital ectropion
• Q10.2
  Congenital entropion
• Q10.3
  Other congenital malformations of eyelid
• Q10.4
  Absence and agenesis of lacrimal apparatus
• Q10.5
  Congenital stenosis and stricture of lacrimal duct
• Q10.6
  Other congenital malformations of lacrimal apparatus
• Q10.7
  Congenital malformation of orbit
• Q11.0
  Cystic eyeball
• Q11.1
  Other anophthalmos
• Q11.2
  Microphthalmos
• Q11.3
  Macrophthalmos
• Q12.0
  Congenital cataract
• Q12.1
  Congenital displaced lens
• Q12.2
  Coloboma of lens
• Q12.3
  Congenital aphakia
• Q12.4
  Spherophakia
• Q12.8
  Other congenital lens malformations
• Q12.9
  Congenital lens malformation, unspecified
• Q13.0
  Coloboma of iris
• Q13.1
  Absence of iris
• Q13.2
  Other congenital malformations of iris
• Q13.3
  Congenital corneal opacity
• Q13.4
  Other congenital corneal malformations
• Q13.5
  Blue sclera
• Q13.81
  Rieger's anomaly
• Q13.89
  Other congenital malformations of anterior segment of eye
• Q13.9
  Congenital malformation of anterior segment of eye, unspecified
• Q14.0
  Congenital malformation of vitreous humor
• Q14.1
  Congenital malformation of retina
• Q14.2
  Congenital malformation of optic disc
• Q14.3
  Congenital malformation of choroid
• Q14.8
  Other congenital malformations of posterior segment of eye
• Q14.9
  Congenital malformation of posterior segment of eye, unspecified
• Q15.0
  Congenital glaucoma
• Q15.8
  Other specified congenital malformations of eye
• Q15.9
  Congenital malformation of eye, unspecified
• Q16.0
  Congenital absence of (ear) auricle
• Q16.1
  Congenital absence, atresia and stricture of auditory canal (external)