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ECI Qualifying Diagnosis Search


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Diagnosis Results

Qualifying Diagnosis Codes have the following notation: < Q >

    • Q00 Anencephaly and similar malformations
    • 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
    • Q99 Other chromosome abnormalities, not elsewhere classified
      • Q99.2 <Q> Fragile X chromosome
      • Q99.9 <Q> Chromosomal abnormality, unspecified