Billable/Specific ICD-10-CM Codes - Page 208

There are 35,750 ICD-10-CM codes which are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code.

  • Q77.5 - Diastrophic dysplasia
  • Q77.6 - Chondroectodermal dysplasia
  • Q77.7 - Spondyloepiphyseal dysplasia
  • Q77.8 - Other osteochondrodysplasia with defects of growth of tubular bones and spine
  • Q77.9 - Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
  • Q78.0 - Osteogenesis imperfecta
  • Q78.1 - Polyostotic fibrous dysplasia
  • Q78.2 - Osteopetrosis
  • Q78.3 - Progressive diaphyseal dysplasia
  • Q78.4 - Enchondromatosis
  • Q78.5 - Metaphyseal dysplasia
  • Q78.6 - Multiple congenital exostoses
  • Q78.8 - Other specified osteochondrodysplasias
  • Q78.9 - Osteochondrodysplasia, unspecified
  • Q79.0 - Congenital diaphragmatic hernia
  • Q79.1 - Other congenital malformations of diaphragm
  • Q79.2 - Exomphalos
  • Q79.3 - Gastroschisis
  • 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
  • Q85.81 - PTEN hamartoma tumor syndrome
  • Q85.82 - Other Cowden syndrome
  • Q85.83 - Von Hippel-Lindau syndrome
  • Q85.89 - 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 syndrome, unspecified
  • Q87.410 - Marfan syndrome with aortic dilation
  • Q87.418 - Marfan syndrome with other cardiovascular manifestations
  • Q87.42 - Marfan syndrome with ocular manifestations
  • Q87.43 - Marfan syndrome with skeletal manifestation
  • Q87.5 - Other congenital malformation syndromes with other skeletal changes
  • Q87.81 - Alport syndrome
  • Q87.82 - Arterial tortuosity syndrome
  • Q87.83 - Bardet-Biedl syndrome
  • Q87.84 - Laurence-Moon syndrome
  • Q87.85 - MED13L syndrome
  • Q87.86 - Kleefstra 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