Present On Admission Exempt Codes
ICD-10-CM diagnosis codes exempt from POA reporting based on the official FY2027 CMS POA exempt list.
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Codes on this list
38,399 codes, page 15 of 384.
- Q79.2Exomphalos
- Q79.3Gastroschisis
- Q79.4Prune belly syndrome
- Q79.51Congenital hernia of bladder
- Q79.59Other congenital malformations of abdominal wall
- Q79.60Ehlers-Danlos syndrome, unspecified
- Q79.61Classical Ehlers-Danlos syndrome
- Q79.62Hypermobile Ehlers-Danlos syndrome
- Q79.63Vascular Ehlers-Danlos syndrome
- Q79.69Other Ehlers-Danlos syndromes
- Q79.8Other congenital malformations of musculoskeletal system
- Q79.9Congenital malformation of musculoskeletal system, unspecified
- Q80.0Ichthyosis vulgaris
- Q80.1X-linked ichthyosis
- Q80.2Lamellar ichthyosis
- Q80.3Congenital bullous ichthyosiform erythroderma
- Q80.4Harlequin fetus
- Q80.8Other congenital ichthyosis
- Q80.9Congenital ichthyosis, unspecified
- Q81.0Epidermolysis bullosa simplex
- Q81.1Epidermolysis bullosa letalis
- Q81.2Epidermolysis bullosa dystrophica
- Q81.8Other epidermolysis bullosa
- Q81.9Epidermolysis bullosa, unspecified
- Q82.0Hereditary lymphedema
- Q82.1Xeroderma pigmentosum
- Q82.2Congenital cutaneous mastocytosis
- Q82.3Incontinentia pigmenti
- Q82.4Ectodermal dysplasia (anhidrotic)
- Q82.5Congenital non-neoplastic nevus
- Q82.6Congenital sacral dimple
- Q82.8Other specified congenital malformations of skin
- Q82.9Congenital malformation of skin, unspecified
- Q83.0Congenital absence of breast with absent nipple
- Q83.1Accessory breast
- Q83.2Absent nipple
- Q83.3Accessory nipple
- Q83.8Other congenital malformations of breast
- Q83.9Congenital malformation of breast, unspecified
- Q84.0Congenital alopecia
- Q84.1Congenital morphological disturbances of hair, not elsewhere classified
- Q84.2Other congenital malformations of hair
- Q84.3Anonychia
- Q84.4Congenital leukonychia
- Q84.5Enlarged and hypertrophic nails
- Q84.6Other congenital malformations of nails
- Q84.8Other specified congenital malformations of integument
- Q84.9Congenital malformation of integument, unspecified
- Q85.00Neurofibromatosis, unspecified
- Q85.01Neurofibromatosis, type 1
- Q85.02Neurofibromatosis, type 2
- Q85.03Schwannomatosis
- Q85.09Other neurofibromatosis
- Q85.1Tuberous sclerosis
- Q85.81PTEN hamartoma tumor syndrome
- Q85.82Other Cowden syndrome
- Q85.83Von Hippel-Lindau syndrome
- Q85.89Other phakomatoses, not elsewhere classified
- Q85.9Phakomatosis, unspecified
- Q86.0Fetal alcohol syndrome (dysmorphic)
- Q86.1Fetal hydantoin syndrome
- Q86.2Dysmorphism due to warfarin
- Q86.8Other congenital malformation syndromes due to known exogenous causes
- Q87.0Congenital malformation syndromes predominantly affecting facial appearance
- Q87.11Prader-Willi syndrome
- Q87.19Other congenital malformation syndromes predominantly associated with short stature
- Q87.2Congenital malformation syndromes predominantly involving limbs
- Q87.3Congenital malformation syndromes involving early overgrowth
- Q87.40Marfan syndrome, unspecified
- Q87.410Marfan syndrome with aortic dilation
- Q87.418Marfan syndrome with other cardiovascular manifestations
- Q87.42Marfan syndrome with ocular manifestations
- Q87.43Marfan syndrome with skeletal manifestation
- Q87.5Other congenital malformation syndromes with other skeletal changes
- Q87.81Alport syndrome
- Q87.82Arterial tortuosity syndrome
- Q87.83Bardet-Biedl syndrome
- Q87.84Laurence-Moon syndrome
- Q87.85MED13L syndrome
- Q87.86Kleefstra syndrome
- Q87.87Hao-Fountain Syndrome
- Q87.88CTNNB1 syndrome
- Q87.89Other specified congenital malformation syndromes, not elsewhere classified
- Q87.ALoeys-Dietz syndrome
- Q89.01Asplenia (congenital)
- Q89.09Congenital malformations of spleen
- Q89.1Congenital malformations of adrenal gland
- Q89.2Congenital malformations of other endocrine glands
- Q89.3Situs inversus
- Q89.4Conjoined twins
- Q89.7Multiple congenital malformations, not elsewhere classified
- Q89.81Kabuki syndrome
- Q89.89Other specified congenital malformations
- Q89.9Congenital malformation, unspecified
- Q90.0Trisomy 21, nonmosaicism (meiotic nondisjunction)
- Q90.1Trisomy 21, mosaicism (mitotic nondisjunction)
- Q90.2Trisomy 21, translocation
- Q90.9Down syndrome, unspecified
- Q91.0Trisomy 18, nonmosaicism (meiotic nondisjunction)
- Q91.1Trisomy 18, mosaicism (mitotic nondisjunction)