1. ICD10Data
›
2. Rules
›
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 37,258 ICD-10-CM codes are considered exempt from POA reporting.

Displaying codes 601-700 of 37,258:

• Q27.33
  Arteriovenous malformation of digestive system vessel
• Q27.34
  Arteriovenous malformation of renal vessel
• Q27.39
  Arteriovenous malformation, other site
• Q27.4
  Congenital phlebectasia
• Q27.8
  Other specified congenital malformations of peripheral vascular system
• Q27.9
  Congenital malformation of peripheral vascular system, unspecified
• Q28.0
  Arteriovenous malformation of precerebral vessels
• Q28.1
  Other malformations of precerebral vessels
• Q28.2
  Arteriovenous malformation of cerebral vessels
• Q28.3
  Other malformations of cerebral vessels
• Q28.8
  Other specified congenital malformations of circulatory system
• Q28.9
  Congenital malformation of circulatory system, unspecified
• Q30.0
  Choanal atresia
• Q30.1
  Agenesis and underdevelopment of nose
• Q30.2
  Fissured, notched and cleft nose
• Q30.3
  Congenital perforated nasal septum
• Q30.8
  Other congenital malformations of nose
• Q30.9
  Congenital malformation of nose, unspecified
• Q31.0
  Web of larynx
• Q31.1
  Congenital subglottic stenosis
• Q31.2
  Laryngeal hypoplasia
• Q31.3
  Laryngocele
• Q31.5
  Congenital laryngomalacia
• Q31.8
  Other congenital malformations of larynx
• Q31.9
  Congenital malformation of larynx, unspecified
• Q32.0
  Congenital tracheomalacia
• Q32.1
  Other congenital malformations of trachea
• Q32.2
  Congenital bronchomalacia
• Q32.3
  Congenital stenosis of bronchus
• Q32.4
  Other congenital malformations of bronchus
• Q33.0
  Congenital cystic lung
• Q33.1
  Accessory lobe of lung
• Q33.2
  Sequestration of lung
• Q33.3
  Agenesis of lung
• Q33.4
  Congenital bronchiectasis
• Q33.5
  Ectopic tissue in lung
• Q33.6
  Congenital hypoplasia and dysplasia of lung
• Q33.8
  Other congenital malformations of lung
• Q33.9
  Congenital malformation of lung, unspecified
• Q34.0
  Anomaly of pleura
• Q34.1
  Congenital cyst of mediastinum
• Q34.8
  Other specified congenital malformations of respiratory system
• Q34.9
  Congenital malformation of respiratory system, unspecified
• Q35.1
  Cleft hard palate
• Q35.3
  Cleft soft palate
• Q35.5
  Cleft hard palate with cleft soft palate
• Q35.7
  Cleft uvula
• Q35.9
  Cleft palate, unspecified
• Q36.0
  Cleft lip, bilateral
• Q36.1
  Cleft lip, median
• Q36.9
  Cleft lip, unilateral
• Q37.0
  Cleft hard palate with bilateral cleft lip
• Q37.1
  Cleft hard palate with unilateral cleft lip
• Q37.2
  Cleft soft palate with bilateral cleft lip
• Q37.3
  Cleft soft palate with unilateral cleft lip
• Q37.4
  Cleft hard and soft palate with bilateral cleft lip
• Q37.5
  Cleft hard and soft palate with unilateral cleft lip
• Q37.8
  Unspecified cleft palate with bilateral cleft lip
• Q37.9
  Unspecified cleft palate with unilateral cleft lip
• Q38.0
  Congenital malformations of lips, not elsewhere classified
• Q38.1
  Ankyloglossia
• Q38.2
  Macroglossia
• Q38.3
  Other congenital malformations of tongue
• Q38.4
  Congenital malformations of salivary glands and ducts
• Q38.5
  Congenital malformations of palate, not elsewhere classified
• Q38.6
  Other congenital malformations of mouth
• Q38.7
  Congenital pharyngeal pouch
• Q38.8
  Other congenital malformations of pharynx
• Q39.0
  Atresia of esophagus without fistula
• Q39.1
  Atresia of esophagus with tracheo-esophageal fistula
• Q39.2
  Congenital tracheo-esophageal fistula without atresia
• Q39.3
  Congenital stenosis and stricture of esophagus
• Q39.4
  Esophageal web
• Q39.5
  Congenital dilatation of esophagus
• Q39.6
  Congenital diverticulum of esophagus
• Q39.8
  Other congenital malformations of esophagus
• Q39.9
  Congenital malformation of esophagus, unspecified
• Q40.0
  Congenital hypertrophic pyloric stenosis
• Q40.1
  Congenital hiatus hernia
• Q40.2
  Other specified congenital malformations of stomach
• Q40.3
  Congenital malformation of stomach, unspecified
• Q40.8
  Other specified congenital malformations of upper alimentary tract
• Q40.9
  Congenital malformation of upper alimentary tract, unspecified
• Q41.0
  Congenital absence, atresia and stenosis of duodenum
• Q41.1
  Congenital absence, atresia and stenosis of jejunum
• Q41.2
  Congenital absence, atresia and stenosis of ileum
• Q41.8
  Congenital absence, atresia and stenosis of other specified parts of small intestine
• Q41.9
  Congenital absence, atresia and stenosis of small intestine, part unspecified
• Q42.0
  Congenital absence, atresia and stenosis of rectum with fistula
• Q42.1
  Congenital absence, atresia and stenosis of rectum without fistula
• Q42.2
  Congenital absence, atresia and stenosis of anus with fistula
• Q42.3
  Congenital absence, atresia and stenosis of anus without fistula
• Q42.8
  Congenital absence, atresia and stenosis of other parts of large intestine
• Q42.9
  Congenital absence, atresia and stenosis of large intestine, part unspecified
• Q43.0
  Meckel's diverticulum (displaced) (hypertrophic)
• Q43.1
  Hirschsprung's disease
• Q43.2
  Other congenital functional disorders of colon
• Q43.3
  Congenital malformations of intestinal fixation
• Q43.4
  Duplication of intestine
• Q43.5
  Ectopic anus