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 37,075 ICD-10-CM codes are considered exempt from POA reporting.

Displaying codes 1,101-1,200 of 37,075:

  • Q79.4
    Prune belly syndrome
  • Q79.51
    Congenital hernia of bladder
  • Q79.59
    Other congenital malformations of abdominal wall
  • Q79.60
    Ehlers-Danlos syndrome, unspecified
  • Q79.61
    Classical Ehlers-Danlos syndrome
  • Q79.62
    Hypermobile Ehlers-Danlos syndrome
  • Q79.63
    Vascular Ehlers-Danlos syndrome
  • Q79.69
    Other Ehlers-Danlos syndromes
  • Q79.8
    Other congenital malformations of musculoskeletal system
  • Q79.9
    Congenital malformation of musculoskeletal system, unspecified
  • Q80.0
    Ichthyosis vulgaris
  • Q80.1
    X-linked ichthyosis
  • Q80.2
    Lamellar ichthyosis
  • Q80.3
    Congenital bullous ichthyosiform erythroderma
  • Q80.4
    Harlequin fetus
  • Q80.8
    Other congenital ichthyosis
  • Q80.9
    Congenital ichthyosis, unspecified
  • Q81.0
    Epidermolysis bullosa simplex
  • Q81.1
    Epidermolysis bullosa letalis
  • Q81.2
    Epidermolysis bullosa dystrophica
  • Q81.8
    Other epidermolysis bullosa
  • Q81.9
    Epidermolysis bullosa, unspecified
  • Q82.0
    Hereditary lymphedema
  • Q82.1
    Xeroderma pigmentosum
  • Q82.2
    Congenital cutaneous mastocytosis
  • Q82.3
    Incontinentia pigmenti
  • Q82.4
    Ectodermal dysplasia (anhidrotic)
  • Q82.5
    Congenital non-neoplastic nevus
  • Q82.6
    Congenital sacral dimple
  • Q82.8
    Other specified congenital malformations of skin
  • Q82.9
    Congenital malformation of skin, unspecified
  • Q83.0
    Congenital absence of breast with absent nipple
  • Q83.1
    Accessory breast
  • Q83.2
    Absent nipple
  • Q83.3
    Accessory nipple
  • Q83.8
    Other congenital malformations of breast
  • Q83.9
    Congenital malformation of breast, unspecified
  • Q84.0
    Congenital alopecia
  • Q84.1
    Congenital morphological disturbances of hair, not elsewhere classified
  • Q84.2
    Other congenital malformations of hair
  • Q84.3
    Anonychia
  • Q84.4
    Congenital leukonychia
  • Q84.5
    Enlarged and hypertrophic nails
  • Q84.6
    Other congenital malformations of nails
  • Q84.8
    Other specified congenital malformations of integument
  • Q84.9
    Congenital malformation of integument, unspecified
  • Q85.00
    Neurofibromatosis, unspecified
  • Q85.01
    Neurofibromatosis, type 1
  • Q85.02
    Neurofibromatosis, type 2
  • Q85.03
    Schwannomatosis
  • Q85.09
    Other neurofibromatosis
  • Q85.1
    Tuberous sclerosis
  • Q85.8
    Other phakomatoses, not elsewhere classified
  • Q85.9
    Phakomatosis, unspecified
  • Q86.0
    Fetal alcohol syndrome (dysmorphic)
  • Q86.1
    Fetal hydantoin syndrome
  • Q86.2
    Dysmorphism due to warfarin
  • Q86.8
    Other congenital malformation syndromes due to known exogenous causes
  • Q87.0
    Congenital malformation syndromes predominantly affecting facial appearance
  • Q87.11
    Prader-Willi syndrome
  • Q87.19
    Other congenital malformation syndromes predominantly associated with short stature
  • Q87.2
    Congenital malformation syndromes predominantly involving limbs
  • Q87.3
    Congenital malformation syndromes involving early overgrowth
  • Q87.40
    Marfan's syndrome, unspecified
  • Q87.410
    Marfan's syndrome with aortic dilation
  • Q87.418
    Marfan's syndrome with other cardiovascular manifestations
  • Q87.42
    Marfan's syndrome with ocular manifestations
  • Q87.43
    Marfan's syndrome with skeletal manifestation
  • Q87.5
    Other congenital malformation syndromes with other skeletal changes
  • Q87.81
    Alport syndrome
  • Q87.82
    Arterial tortuosity syndrome
  • Q87.89
    Other specified congenital malformation syndromes, not elsewhere classified
  • Q89.01
    Asplenia (congenital)
  • Q89.09
    Congenital malformations of spleen
  • Q89.1
    Congenital malformations of adrenal gland
  • Q89.2
    Congenital malformations of other endocrine glands
  • Q89.3
    Situs inversus
  • Q89.4
    Conjoined twins
  • Q89.7
    Multiple congenital malformations, not elsewhere classified
  • Q89.8
    Other specified congenital malformations
  • Q89.9
    Congenital malformation, unspecified
  • Q90.0
    Trisomy 21, nonmosaicism (meiotic nondisjunction)
  • Q90.1
    Trisomy 21, mosaicism (mitotic nondisjunction)
  • Q90.2
    Trisomy 21, translocation
  • Q90.9
    Down syndrome, unspecified
  • Q91.0
    Trisomy 18, nonmosaicism (meiotic nondisjunction)
  • Q91.1
    Trisomy 18, mosaicism (mitotic nondisjunction)
  • Q91.2
    Trisomy 18, translocation
  • Q91.3
    Trisomy 18, unspecified
  • Q91.4
    Trisomy 13, nonmosaicism (meiotic nondisjunction)
  • Q91.5
    Trisomy 13, mosaicism (mitotic nondisjunction)
  • Q91.6
    Trisomy 13, translocation
  • Q91.7
    Trisomy 13, unspecified
  • Q92.0
    Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
  • Q92.1
    Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
  • Q92.2
    Partial trisomy
  • Q92.5
    Duplications with other complex rearrangements
  • Q92.61
    Marker chromosomes in normal individual
  • Q92.62
    Marker chromosomes in abnormal individual
  • Q92.7
    Triploidy and polyploidy
ICD-10-CM Code Q79.4

Prune belly syndrome

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital prolapse of bladder mucosa
  • Eagle-Barrett syndrome
ICD-10-CM Code Q79.51

Congenital hernia of bladder

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q79.59

Other congenital malformations of abdominal wall

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q79.60

Ehlers-Danlos syndrome, unspecified

    2020 - New Code Billable/Specific Code POA Exempt
ICD-10-CM Code Q79.61

Classical Ehlers-Danlos syndrome

    2020 - New Code Billable/Specific Code POA Exempt
Applicable To
  • Classical EDS (cEDS)
ICD-10-CM Code Q79.62

Hypermobile Ehlers-Danlos syndrome

    2020 - New Code Billable/Specific Code POA Exempt
Applicable To
  • Hypermobile EDS (hEDS)
ICD-10-CM Code Q79.63

Vascular Ehlers-Danlos syndrome

    2020 - New Code Billable/Specific Code POA Exempt
Applicable To
  • Vascular EDS (vEDS)
ICD-10-CM Code Q79.69

Other Ehlers-Danlos syndromes

    2020 - New Code Billable/Specific Code POA Exempt
ICD-10-CM Code Q79.8

Other congenital malformations of musculoskeletal system

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Absence of muscle
  • Absence of tendon
  • Accessory muscle
  • Amyotrophia congenita
  • Congenital constricting bands
  • Congenital shortening of tendon
  • Poland syndrome
ICD-10-CM Code Q79.9

Congenital malformation of musculoskeletal system, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital anomaly of musculoskeletal system NOS
  • Congenital deformity of musculoskeletal system NOS
ICD-10-CM Code Q80.0

Ichthyosis vulgaris

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q80.1

X-linked ichthyosis

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q80.2

Lamellar ichthyosis

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Collodion baby
ICD-10-CM Code Q80.3

Congenital bullous ichthyosiform erythroderma

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q80.4

Harlequin fetus

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q80.8

Other congenital ichthyosis

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q80.9

Congenital ichthyosis, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q81.0

Epidermolysis bullosa simplex

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Type 1 Excludes
ICD-10-CM Code Q81.1

Epidermolysis bullosa letalis

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Herlitz' syndrome
ICD-10-CM Code Q81.2

Epidermolysis bullosa dystrophica

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q81.8

Other epidermolysis bullosa

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q81.9

Epidermolysis bullosa, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q82.0

Hereditary lymphedema

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q82.1

Xeroderma pigmentosum

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q82.2

Congenital cutaneous mastocytosis

    2016 2017 2018 - Revised Code 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital diffuse cutaneous mastocytosis
  • Congenital maculopapular cutaneous mastocytosis
  • Congenital urticaria pigmentosa
Type 1 Excludes
  • cutaneous mastocytosis NOS (D47.01)
  • diffuse cutaneous mastocytosis (with onset after newborn period) (D47.01)
  • malignant mastocytosis (C96.2-)
  • systemic mastocytosis (D47.02)
  • urticaria pigmentosa (non-congenital) (with onset after newborn period) (D47.01)
ICD-10-CM Code Q82.3

Incontinentia pigmenti

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q82.4

Ectodermal dysplasia (anhidrotic)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Type 1 Excludes
  • Ellis-van Creveld syndrome (Q77.6)
ICD-10-CM Code Q82.5

Congenital non-neoplastic nevus

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Birthmark NOS
  • Flammeus Nevus
  • Portwine Nevus
  • Sanguineous Nevus
  • Strawberry Nevus
  • Vascular Nevus NOS
  • Verrucous Nevus
Type 2 Excludes
ICD-10-CM Code Q82.6

Congenital sacral dimple

    2017 - New Code 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Parasacral dimple
Type 2 Excludes
  • pilonidal cyst with abscess (L05.01)
  • pilonidal cyst without abscess (L05.91)
ICD-10-CM Code Q82.8

Other specified congenital malformations of skin

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Abnormal palmar creases
  • Accessory skin tags
  • Benign familial pemphigus [Hailey-Hailey]
  • Congenital poikiloderma
  • Cutis laxa (hyperelastica)
  • Dermatoglyphic anomalies
  • Inherited keratosis palmaris et plantaris
  • Keratosis follicularis [Darier-White]
Type 1 Excludes
  • Ehlers-Danlos syndrome (Q79.6-)
ICD-10-CM Code Q82.9

Congenital malformation of skin, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q83.0

Congenital absence of breast with absent nipple

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q83.1

Accessory breast

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Supernumerary breast
ICD-10-CM Code Q83.2

Absent nipple

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q83.3

Accessory nipple

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Supernumerary nipple
ICD-10-CM Code Q83.8

Other congenital malformations of breast

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q83.9

Congenital malformation of breast, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q84.0

Congenital alopecia

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital atrichosis
ICD-10-CM Code Q84.1

Congenital morphological disturbances of hair, not elsewhere classified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Beaded hair
  • Monilethrix
  • Pili annulati
Type 1 Excludes
  • Menkes' kinky hair syndrome (E83.0)
ICD-10-CM Code Q84.2

Other congenital malformations of hair

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital hypertrichosis
  • Congenital malformation of hair NOS
  • Persistent lanugo
ICD-10-CM Code Q84.3

Anonychia

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Type 1 Excludes
  • nail patella syndrome (Q87.2)
ICD-10-CM Code Q84.4

Congenital leukonychia

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q84.5

Enlarged and hypertrophic nails

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital onychauxis
  • Pachyonychia
ICD-10-CM Code Q84.6

Other congenital malformations of nails

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital clubnail
  • Congenital koilonychia
  • Congenital malformation of nail NOS
ICD-10-CM Code Q84.8

Other specified congenital malformations of integument

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Aplasia cutis congenita
ICD-10-CM Code Q84.9

Congenital malformation of integument, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital anomaly of integument NOS
  • Congenital deformity of integument NOS
ICD-10-CM Code Q85.00

Neurofibromatosis, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q85.01

Neurofibromatosis, type 1

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Von Recklinghausen disease
ICD-10-CM Code Q85.02

Neurofibromatosis, type 2

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Acoustic neurofibromatosis
ICD-10-CM Code Q85.03

Schwannomatosis

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q85.09

Other neurofibromatosis

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q85.1

Tuberous sclerosis

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Bourneville's disease
  • Epiloia
ICD-10-CM Code Q85.8

Other phakomatoses, not elsewhere classified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Peutz-Jeghers Syndrome
  • Sturge-Weber(-Dimitri) syndrome
  • von Hippel-Lindau syndrome
Type 1 Excludes
  • Meckel-Gruber syndrome (Q61.9)
ICD-10-CM Code Q85.9

Phakomatosis, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Hamartosis NOS
ICD-10-CM Code Q86.0

Fetal alcohol syndrome (dysmorphic)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q86.1

Fetal hydantoin syndrome

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Meadow's syndrome
ICD-10-CM Code Q86.2

Dysmorphism due to warfarin

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q86.8

Other congenital malformation syndromes due to known exogenous causes

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.0

Congenital malformation syndromes predominantly affecting facial appearance

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Acrocephalopolysyndactyly
  • Acrocephalosyndactyly [Apert]
  • Cryptophthalmos syndrome
  • Cyclopia
  • Goldenhar syndrome
  • Moebius syndrome
  • Oro-facial-digital syndrome
  • Robin syndrome
  • Whistling face
ICD-10-CM Code Q87.11

Prader-Willi syndrome

    2020 - New Code Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.19

Other congenital malformation syndromes predominantly associated with short stature

    2020 - New Code Billable/Specific Code POA Exempt
Applicable To
  • Aarskog syndrome
  • Cockayne syndrome
  • De Lange syndrome
  • Dubowitz syndrome
  • Noonan syndrome
  • Robinow-Silverman-Smith syndrome
  • Russell-Silver syndrome
  • Seckel syndrome
ICD-10-CM Code Q87.2

Congenital malformation syndromes predominantly involving limbs

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Holt-Oram syndrome
  • Klippel-Trenaunay-Weber syndrome
  • Nail patella syndrome
  • Rubinstein-Taybi syndrome
  • Sirenomelia syndrome
  • Thrombocytopenia with absent radius [TAR] syndrome
  • VATER syndrome
ICD-10-CM Code Q87.3

Congenital malformation syndromes involving early overgrowth

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Beckwith-Wiedemann syndrome
  • Sotos syndrome
  • Weaver syndrome
ICD-10-CM Code Q87.40

Marfan's syndrome, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.410

Marfan's syndrome with aortic dilation

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.418

Marfan's syndrome with other cardiovascular manifestations

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.42

Marfan's syndrome with ocular manifestations

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.43

Marfan's syndrome with skeletal manifestation

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.5

Other congenital malformation syndromes with other skeletal changes

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.81

Alport syndrome

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Use Additional
  • code to identify stage of chronic kidney disease (N18.1-N18.6)
ICD-10-CM Code Q87.82

Arterial tortuosity syndrome

    2017 - New Code 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q87.89

Other specified congenital malformation syndromes, not elsewhere classified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Laurence-Moon (-Bardet)-Biedl syndrome
ICD-10-CM Code Q89.01

Asplenia (congenital)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q89.09

Congenital malformations of spleen

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital splenomegaly
ICD-10-CM Code Q89.1

Congenital malformations of adrenal gland

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Type 1 Excludes
  • adrenogenital disorders (E25.-)
  • congenital adrenal hyperplasia (E25.0)
ICD-10-CM Code Q89.2

Congenital malformations of other endocrine glands

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital malformation of parathyroid or thyroid gland
  • Persistent thyroglossal duct
  • Thyroglossal cyst
Type 1 Excludes
  • congenital goiter (E03.0)
  • congenital hypothyroidism (E03.1)
ICD-10-CM Code Q89.3

Situs inversus

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Dextrocardia with situs inversus
  • Mirror-image atrial arrangement with situs inversus
  • Situs inversus or transversus abdominalis
  • Situs inversus or transversus thoracis
  • Transposition of abdominal viscera
  • Transposition of thoracic viscera
Type 1 Excludes
ICD-10-CM Code Q89.4

Conjoined twins

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Craniopagus
  • Dicephaly
  • Pygopagus
  • Thoracopagus
ICD-10-CM Code Q89.7

Multiple congenital malformations, not elsewhere classified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Multiple congenital anomalies NOS
  • Multiple congenital deformities NOS
Type 1 Excludes
  • congenital malformation syndromes affecting multiple systems (Q87.-)
ICD-10-CM Code Q89.8

Other specified congenital malformations

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Use Additional
  • code(s) to identify all associated manifestations
ICD-10-CM Code Q89.9

Congenital malformation, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Congenital anomaly NOS
  • Congenital deformity NOS
ICD-10-CM Code Q90.0

Trisomy 21, nonmosaicism (meiotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q90.1

Trisomy 21, mosaicism (mitotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q90.2

Trisomy 21, translocation

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q90.9

Down syndrome, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Trisomy 21 NOS
ICD-10-CM Code Q91.0

Trisomy 18, nonmosaicism (meiotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q91.1

Trisomy 18, mosaicism (mitotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q91.2

Trisomy 18, translocation

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q91.3

Trisomy 18, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q91.4

Trisomy 13, nonmosaicism (meiotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q91.5

Trisomy 13, mosaicism (mitotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q91.6

Trisomy 13, translocation

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q91.7

Trisomy 13, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q92.0

Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q92.1

Whole chromosome trisomy, mosaicism (mitotic nondisjunction)

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q92.2

Partial trisomy

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Less than whole arm duplicated
  • Whole arm or more duplicated
Type 1 Excludes
  • partial trisomy due to unbalanced translocation (Q92.5)
ICD-10-CM Code Q92.5

Duplications with other complex rearrangements

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
Applicable To
  • Partial trisomy due to unbalanced translocations
Code Also
  • any associated deletions due to unbalanced translocations, inversions and insertions (Q93.7)
ICD-10-CM Code Q92.61

Marker chromosomes in normal individual

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q92.62

Marker chromosomes in abnormal individual

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
ICD-10-CM Code Q92.7

Triploidy and polyploidy

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt