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 37,658 ICD-10-CM codes are considered exempt from POA reporting.

Displaying codes 701-800 of 37,658:

• 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
• Q43.6
  Congenital fistula of rectum and anus
• Q43.7
  Persistent cloaca
• Q43.8
  Other specified congenital malformations of intestine
• Q43.9
  Congenital malformation of intestine, unspecified
• Q44.0
  Agenesis, aplasia and hypoplasia of gallbladder
• Q44.1
  Other congenital malformations of gallbladder
• Q44.2
  Atresia of bile ducts
• Q44.3
  Congenital stenosis and stricture of bile ducts
• Q44.4
  Choledochal cyst
• Q44.5
  Other congenital malformations of bile ducts
• Q44.6
  Cystic disease of liver
• Q44.7
  Other congenital malformations of liver
• Q45.0
  Agenesis, aplasia and hypoplasia of pancreas
• Q45.1
  Annular pancreas
• Q45.2
  Congenital pancreatic cyst
• Q45.3
  Other congenital malformations of pancreas and pancreatic duct
• Q45.8
  Other specified congenital malformations of digestive system
• Q45.9
  Congenital malformation of digestive system, unspecified
• Q50.01
  Congenital absence of ovary, unilateral
• Q50.02
  Congenital absence of ovary, bilateral
• Q50.1
  Developmental ovarian cyst
• Q50.2
  Congenital torsion of ovary
• Q50.31
  Accessory ovary
• Q50.32
  Ovarian streak
• Q50.39
  Other congenital malformation of ovary
• Q50.4
  Embryonic cyst of fallopian tube
• Q50.5
  Embryonic cyst of broad ligament
• Q50.6
  Other congenital malformations of fallopian tube and broad ligament
• Q51.0
  Agenesis and aplasia of uterus
• Q51.10
  Doubling of uterus with doubling of cervix and vagina without obstruction
• Q51.11
  Doubling of uterus with doubling of cervix and vagina with obstruction
• Q51.21
  Complete doubling of uterus
• Q51.22
  Partial doubling of uterus
• Q51.28
  Other and unspecified doubling of uterus
• Q51.3
  Bicornate uterus
• Q51.4
  Unicornate uterus
• Q51.5
  Agenesis and aplasia of cervix
• Q51.6
  Embryonic cyst of cervix
• Q51.7
  Congenital fistulae between uterus and digestive and urinary tracts
• Q51.810
  Arcuate uterus
• Q51.811
  Hypoplasia of uterus
• Q51.818
  Other congenital malformations of uterus
• Q51.820
  Cervical duplication
• Q51.821
  Hypoplasia of cervix
• Q51.828
  Other congenital malformations of cervix
• Q51.9
  Congenital malformation of uterus and cervix, unspecified
• Q52.0
  Congenital absence of vagina
• Q52.10
  Doubling of vagina, unspecified
• Q52.11
  Transverse vaginal septum
• Q52.120
  Longitudinal vaginal septum, nonobstructing
• Q52.121
  Longitudinal vaginal septum, obstructing, right side
• Q52.122
  Longitudinal vaginal septum, obstructing, left side
• Q52.123
  Longitudinal vaginal septum, microperforate, right side
• Q52.124
  Longitudinal vaginal septum, microperforate, left side
• Q52.129
  Other and unspecified longitudinal vaginal septum
• Q52.2
  Congenital rectovaginal fistula
• Q52.3
  Imperforate hymen
• Q52.4
  Other congenital malformations of vagina
• Q52.5
  Fusion of labia
• Q52.6
  Congenital malformation of clitoris
• Q52.70
  Unspecified congenital malformations of vulva
• Q52.71
  Congenital absence of vulva
• Q52.79
  Other congenital malformations of vulva
• Q52.8
  Other specified congenital malformations of female genitalia
• Q52.9
  Congenital malformation of female genitalia, unspecified
• Q53.00
  Ectopic testis, unspecified
• Q53.01
  Ectopic testis, unilateral
• Q53.02
  Ectopic testes, bilateral
• Q53.10
  Unspecified undescended testicle, unilateral
• Q53.111
  Unilateral intraabdominal testis
• Q53.112
  Unilateral inguinal testis
• Q53.12
  Ectopic perineal testis, unilateral
• Q53.13
  Unilateral high scrotal testis
• Q53.20
  Undescended testicle, unspecified, bilateral
• Q53.211
  Bilateral intraabdominal testes
• Q53.212
  Bilateral inguinal testes
• Q53.22
  Ectopic perineal testis, bilateral
• Q53.23
  Bilateral high scrotal testes
• Q53.9
  Undescended testicle, unspecified
• Q54.0
  Hypospadias, balanic
• Q54.1
  Hypospadias, penile
• Q54.2
  Hypospadias, penoscrotal
• Q54.3
  Hypospadias, perineal
• Q54.4
  Congenital chordee
• Q54.8
  Other hypospadias
• Q54.9
  Hypospadias, unspecified
• Q55.0
  Absence and aplasia of testis
• Q55.1
  Hypoplasia of testis and scrotum
• Q55.20
  Unspecified congenital malformations of testis and scrotum