ECI Qualifying Diagnosis Search

Search Eligible Codes

To search for medically qualifying diagnoses enter the name of the condition or diagnosis code in the search box below and hit search.

An auto-lookup feature will help you narrow your search results.

Diagnosis Results

Qualifying Diagnosis Codes have the following notation: < Q >

• • Q00 Anencephaly and similar malformations
    • Q00.0 <Q> Anencephaly
  • Q01 Encephalocele
    • Q01.0 <Q> Frontal encephalocele
    • Q01.1 <Q> Nasofrontal encephalocele
    • Q01.2 <Q> Occipital encephalocele
    • Q01.8 <Q> Encephalocele of other sites
    • Q01.9 <Q> Encephalocele, unspecified
  • Q02 Microcephaly
  • Q03 Congenital hydrocephalus
    • Q03.1 <Q> Atresia of foramina of Magendie and Luschka
    • Q03.9 <Q> Congenital hydrocephalus, unspecified
  • Q04 Other congenital malformations of brain
    • Q04.0 <Q> Congenital malformations of corpus callosum
    • Q04.2 <Q> Holoprosencephaly
    • Q04.3 <Q> Other reduction deformities of brain
    • Q04.4 <Q> Septo-optic dysplasia of brain
    • Q04.6 <Q> Congenital cerebral cysts
    • Q04.9 <Q> Congenital malformation of brain, unspecified
  • Q05 Spina bifida
    • Q05.0 <Q> Cervical spina bifida with hydrocephalus
    • Q05.1 <Q> Thoracic spina bifida with hydrocephalus
    • Q05.2 <Q> Lumbar spina bifida with hydrocephalus
    • Q05.3 <Q> Sacral spina bifida with hydrocephalus
    • Q05.4 <Q> Unspecified spina bifida with hydrocephalus
    • Q05.5 <Q> Cervical spina bifida without hydrocephalus
    • Q05.6 <Q> Thoracic spina bifida without hydrocephalus
    • Q05.7 <Q> Lumbar spina bifida without hydrocephalus
    • Q05.8 <Q> Sacral spina bifida without hydrocephalus
    • Q05.9 <Q> Spina bifida, unspecified
  • Q06 Other congenital malformations of spinal cord
    • Q06.2 <Q> Diastematomyelia
  • Q07 Other congenital malformations of nervous system
    • Q07.0 Arnold-Chiari syndrome
    • Q07.9 <Q> Congenital malformation of nervous system, unspecified
• • Q11 Anophthalmos, microphthalmos and macrophthalmos
    • Q11.1 <Q> Other anophthalmos
    • Q11.2 <Q> Microphthalmos
  • Q14 Congenital malformations of posterior segment of eye
    • Q14.0 <Q> Congenital malformation of vitreous humor
  • Q15 Other congenital malformations of eye
    • Q15.8 <Q> Other specified congenital malformations of eye
• • Q26 Congenital malformations of great veins
    • Q26.8 <Q> Other congenital malformations of great veins
• • Q35 Cleft palate
    • Q35.1 <Q> Cleft hard palate
    • Q35.3 <Q> Cleft soft palate
    • Q35.5 <Q> Cleft hard palate with cleft soft palate
    • Q35.7 <Q> Cleft uvula
    • Q35.9 <Q> Cleft palate, unspecified
  • Q36 Cleft lip
    • Q36.0 <Q> Cleft lip, bilateral
    • Q36.1 <Q> Cleft lip, median
    • Q36.9 <Q> Cleft lip, unilateral
  • Q37 Cleft palate with cleft lip
    • Q37.0 <Q> Cleft hard palate with bilateral cleft lip
    • Q37.1 <Q> Cleft hard palate with unilateral cleft lip
    • Q37.2 <Q> Cleft soft palate with bilateral cleft lip
    • Q37.3 <Q> Cleft soft palate with unilateral cleft lip
    • Q37.4 <Q> Cleft hard and soft palate with bilateral cleft lip
    • Q37.5 <Q> Cleft hard and soft palate with unilateral cleft lip
    • Q37.8 <Q> Unspecified cleft palate with bilateral cleft lip
    • Q37.9 <Q> Unspecified cleft palate with unilateral cleft lip
• • Q43 Other congenital malformations of intestine
    • Q43.0 <Q> Meckel's diverticulum (displaced) (hypertrophic)
• • Q66 Congenital deformities of feet
    • Q66.8 Other congenital deformities of feet
  • Q67 Congenital musculoskeletal deformities of head, face, spine and chest
    • Q67.3 <Q> Plagiocephaly
  • Q68 Other congenital musculoskeletal deformities
    • Q68.8 <Q> Other specified congenital musculoskeletal deformities
  • Q71 Reduction defects of upper limb
    • Q71.6 Lobster-claw hand
    • Q71.0 Congenital complete absence of upper limb
  • Q72 Reduction defects of lower limb
    • Q72.0 Congenital complete absence of lower limb
  • Q73 Reduction defects of unspecified limb
    • Q73.0 <Q> Congenital absence of unspecified limb(s)
    • Q73.1 <Q> Phocomelia, unspecified limb(s)
    • Q73.8 <Q> Other reduction defects of unspecified limb(s)
  • Q74 Other congenital malformations of limb(s)
    • Q74.3 <Q> Arthrogryposis multiplex congenita
    • Q74.8 <Q> Other specified congenital malformations of limb(s)
  • Q75 Other congenital malformations of skull and face bones
    • Q75.1 <Q> Craniofacial dysostosis
    • Q75.4 <Q> Mandibulofacial dysostosis
  • Q76 Congenital malformations of spine and bony thorax
    • Q76.4 Other congenital malformations of spine, not associated with scoliosis
  • Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
    • Q77.0 <Q> Achondrogenesis
    • Q77.1 <Q> Thanatophoric short stature
    • Q77.3 <Q> Chondrodysplasia punctata
    • Q77.4 <Q> Achondroplasia
    • Q77.5 <Q> Diastrophic dysplasia
    • Q77.8 <Q> Other osteochondrodysplasia with defects of growth of tubular bones and spine
    • Q77.9 <Q> Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
  • Q78 Other osteochondrodysplasias
    • Q78.0 <Q> Osteogenesis imperfecta
    • Q78.1 <Q> Polyostotic fibrous dysplasia
    • Q78.9 <Q> Osteochondrodysplasia, unspecified
  • Q79 Congenital malformations of musculoskeletal system, not elsewhere classified
    • Q79.0 <Q> Congenital diaphragmatic hernia
    • Q79.3 <Q> Gastroschisis
    • Q79.4 <Q> Prune belly syndrome
    • Q79.6 <Q> Ehlers-Danlos syndrome
• • Q80 Congenital ichthyosis
    • Q80.4 <Q> Harlequin fetus
    • Q80.8 <Q> Other congenital ichthyosis
  • Q81 Epidermolysis bullosa
    • Q81.0 <Q> Epidermolysis bullosa simplex
    • Q81.1 <Q> Epidermolysis bullosa letalis
    • Q81.2 <Q> Epidermolysis bullosa dystrophica
    • Q81.8 <Q> Other epidermolysis bullosa
    • Q81.9 <Q> Epidermolysis bullosa, unspecified
  • Q82 Other congenital malformations of skin
    • Q82.1 <Q> Xeroderma pigmentosum
  • Q85 Phakomatoses, not elsewhere classified
    • Q85.0 Neurofibromatosis (nonmalignant)
    • Q85.1 <Q> Tuberous sclerosis
    • Q85.8 <Q> Other phakomatoses, not elsewhere classified
  • Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
    • Q86.0 <Q> Fetal alcohol syndrome (dysmorphic)
  • Q87 Other specified congenital malformation syndromes affecting multiple systems
    • Q87.0 <Q> Congenital malformation syndromes predominantly affecting facial appearance
    • Q87.1 <Q> Congenital malformation syndromes predominantly associated with short stature
    • Q87.2 <Q> Congenital malformation syndromes predominantly involving limbs
    • Q87.3 <Q> Congenital malformation syndromes involving early overgrowth
    • Q87.4 Marfan's syndrome
    • Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
  • Q89 Other congenital malformations, not elsewhere classified
    • Q89.7 <Q> Multiple congenital malformations, not elsewhere classified
    • Q89.8 <Q> Other specified congenital malformations
    • Q89.9 <Q> Congenital malformation, unspecified
• • Q90 Down syndrome
    • Q90.0 <Q> Trisomy 21, nonmosaicism (meiotic nondisjunction)
    • Q90.1 <Q> Trisomy 21, mosaicism (mitotic nondisjunction)
    • Q90.2 <Q> Trisomy 21, translocation
    • Q90.9 <Q> Down syndrome, unspecified
  • Q91 Trisomy 18 and Trisomy 13
    • Q91.0 <Q> Trisomy 18, nonmosaicism (meiotic nondisjunction)
    • Q91.1 <Q> Trisomy 18, mosaicism (mitotic nondisjunction)
    • Q91.2 <Q> Trisomy 18, translocation
    • Q91.3 <Q> Trisomy 18, unspecified
    • Q91.4 <Q> Trisomy 13, nonmosaicism (meiotic nondisjunction)
    • Q91.5 <Q> Trisomy 13, mosaicism (mitotic nondisjunction)
    • Q91.6 <Q> Trisomy 13, translocation
    • Q91.7 <Q> Trisomy 13, unspecified
  • Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified
    • Q92.7 <Q> Triploidy and polyploidy
  • Q93 Monosomies and deletions from the autosomes, not elsewhere classified
    • Q93.4 <Q> Deletion of short arm of chromosome 5
    • Q93.5 <Q> Other deletions of part of a chromosome
    • Q93.8 Other deletions from the autosomes
  • Q96 Turner's syndrome
    • Q96.0 <Q> Karyotype 45, X
    • Q96.1 <Q> Karyotype 46, X iso (Xq)
    • Q96.3 <Q> Mosaicism, 45, X/46, XX or XY
    • Q96.4 <Q> Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
    • Q96.8 <Q> Other variants of Turner's syndrome
    • Q96.9 <Q> Turner's syndrome, unspecified
    • Q96.2 <Q> Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
  • Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
    • Q98.0 <Q> Klinefelter syndrome karyotype 47, XXY
    • Q98.1 <Q> Klinefelter syndrome, male with more than two X chromosomes
    • Q98.3 <Q> Other male with 46, XX karyotype
    • Q98.4 <Q> Klinefelter syndrome, unspecified
    • Q98.5 <Q> Karyotype 47, XYY
  • Q99 Other chromosome abnormalities, not elsewhere classified
    • Q99.2 <Q> Fragile X chromosome
    • Q99.9 <Q> Chromosomal abnormality, unspecified