List of ICD-9 codes 740–759: congenital anomalies

Last updated May 01, 2023

ICD-9 chapters
Chapter	Block	Title
I	001–139	Infectious and Parasitic Diseases
II	140–239	Neoplasms
III	240–279	Endocrine, Nutritional and Metabolic Diseases, and Immunity Disorders
IV	280–289	Diseases of the Blood and Blood-forming Organs
V	290–319	Mental Disorders
VI	320–389	Diseases of the Nervous System and Sense Organs
VII	390–459	Diseases of the Circulatory System
VIII	460–519	Diseases of the Respiratory System
IX	520–579	Diseases of the Digestive System
X	580–629	Diseases of the Genitourinary System
XI	630–679	Complications of Pregnancy, Childbirth, and the Puerperium
XII	680–709	Diseases of the Skin and Subcutaneous Tissue
XIII	710–739	Diseases of the Musculoskeletal System and Connective Tissue
XIV	740–759	Congenital Anomalies
XV	760–779	Certain Conditions originating in the Perinatal Period
XVI	780–799	Symptoms, Signs and Ill-defined Conditions
XVII	800–999	Injury and Poisoning
	E800–E999	Supplementary Classification of External Causes of Injury and Poisoning
	V01–V82	Supplementary Classification of Factors influencing Health Status and Contact with Health Services
	M8000–M9970	Morphology of Neoplasms

This is a shortened version of the fourteenth chapter of the ICD-9: Congenital Anomalies. It covers ICD codes 740 to 759. The full chapter can be found on pages 417 to 437 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1. Both volumes can be downloaded for free from the website of the World Health Organization.

Nervous system (740–742)
Eye, ear, face and neck (743–744)
Circulatory system (745–747)
Respiratory system (748–748)
Digestive system (749–751)
Genital organs (752–752)
Urinary system (753–753)
Musculoskeletal system (754–756)
Integument (757–757)
Chromosomal anomalies (758–758)
Other (759–759)

Nervous system (740–742)

740 Anencephalus and similar anomalies
- 740.0 Anencephalus
741 Spina bifida
742 Other congenital anomalies of nervous system
- 742.1 Microcephalus
- 742.3 Hydrocephalus

Eye, ear, face and neck (743–744)

743 Congenital anomalies of eye
- 743.0 Anophthalmos
  - 743.00 Clinical anophthalmos unspecified
  - 743.03 Cystic eyeball congenital
  - 743.06 Cryptophthalmos
- 743.1 Microphthalmos
- 743.2 Buphthalmos
- 743.3 Congenital cataract and lens anomalies
- 743.4 Coloboma and other anomalies of anterior segment
  - 743.45 Aniridia
- 743.5 Congenital anomalies of posterior segment
- 743.6 Congenital anomalies of eyelids, lacrimal system, and orbit
744 Congenital anomalies of ear, face, and neck
- 744.0 Anomalies of ear causing impairment of hearing
- 744.1 Accessory auricle
- 744.2 Other specified congenital anomalies of ear
  - 744.22 Macrotia
  - 744.23 Microtia
- 744.3 Unspecified congenital anomaly of ear
- 744.4 Branchial cleft cyst or fistula; preauricular sinus
- 744.5 Webbing of neck
- 744.8 Other specified congenital anomalies of face and neck

Circulatory system (745–747)

745 Bulbus cordis anomalies and anomalies of cardiac septal closure
746 Other congenital anomalies of heart
- 746.1 Tricuspid atresia and stenosis congenital
- 746.2 Ebstein's anomaly
- 746.3 Congenital stenosis of aortic valve
- 746.4 Congenital insufficiency of aortic valve
- 746.5 Congenital mitral stenosis
- 746.6 Congenital mitral insufficiency
- 746.7 Hypoplastic left heart syndrome
- 746.8 Other specified congenital anomalies of heart
  - 746.81 Subaortic stenosis congenital
  - 746.82 Cor triatriatum
  - 746.83 Infundibular pulmonic stenosis congenital
  - 746.84 Congenital obstructive anomalies of heart not elsewhere classified
  - 746.85 Coronary artery anomaly congenital
  - 746.86 Congenital heart block
  - 746.87 Malposition of heart and cardiac apex
  - 746.89 Other specified congenital anomalies of heart
    - Brugada syndrome
747 Other congenital anomalies of circulatory system
- 747.1 Coarctation of aorta
  - 747.11 Interruption of aortic arch
- 747.2 Other congenital anomalies of aorta
- 747.3 Congenital anomalies of pulmonary artery
- 747.4 Congenital anomalies of great veins
- 747.5 Absence or hypoplasia of umbilical artery
- 747.6 Arteriovenous malformation, unspec.
- 747.8 Other specified anomalies of circulatory system
- 747.9 Unspecified congenital anomaly of circulatory system

Respiratory system (748–748)

748 Congenital anomalies of respiratory system
- 748.0 Choanal atresia

Digestive system (749–751)

749 Cleft palate
- 749.0 Cleft palate, unspec.
- 749.2 Cleft palate w/ cleft lip
750 Other congenital anomalies of upper alimentary tract
751 Other congenital anomalies of digestive system

Urinary system (753–753)

753 Congenital anomalies of urinary system
- 753.0 Renal agenesis and dysgenesis
- 753.1 Cystic kidney disease
- 753.2 Obstructive defects of renal pelvis and ureter
- 753.3 Other specified anomalies of kidney
  - Renal ectopia
  - Horseshoe kidney
- 753.4 Other specified anomalies of ureter
  - Ectopic ureter
- 753.5 Exstrophy of urinary bladder
- 753.6 Atresia and stenosis of urethra and bladder neck
- 753.7 Anomalies of urachus
  - Urachal cyst
- 753.8 Other specified anomalies of bladder and urethra
- 753.9 Unspecified anomaly of urinary system

Musculoskeletal system (754–756)

754 Certain congenital musculoskeletal deformities
- 754.1 Torticollis, sternomastoid
- 754.3 Dislocation of hip, unilateral
- 754.5 Varus deformities of feet
  - 754.51 Talipes equinovarus
- 754.6 Valgus deformities of feet
- 754.8 Other specified nonteratogenic anomalies
  - 754.81 Pectus excavatum
755 Other congenital anomalies of limbs
- 755.0 Polydactyly
- 755.1 Syndactyly
- 755.5 Other congenital anomalies of upper limb including shoulder girdle
  - 755.54 Madelung's deformity
  - 755.55 Acrocephalosyndactyly
    - Apert syndrome
- 755.9 Limb anomaly, unspec.
756 Other congenital musculoskeletal anomalies

Integument (757–757)

757 Congenital anomalies of the integument
- 757.3 Other specified anomalies of skin
  - 757.32 Birthmarks
  - 757.39 Other specified congenital anomalies of skin
- 757.6 Supernumerary nipple

Chromosomal anomalies (758–758)

758 Chromosomal anomalies
- 758.0 Down syndrome
- 758.1 Patau's syndrome
- 758.2 Edward's syndrome
- 758.3 Autosomal deletion syndromes
- 758.4 Balanced autosomal translocation in normal individual
- 758.5 Other conditions due to autosomal anomalies
- 758.6 Gonadal dysgenesis
  - Turner syndrome
  - XO syndrome
- 758.7 Klinefelter syndrome
- 758.8 Other conditions due to sex chromosome anomalies
  - Snyder–Robinson syndrome (SRS)
- 758.9 Conditions due to anomaly of unspecified chromosome

Other (759–759)

759 Other and unspecified congenital anomalies
- 759.0 Anomalies of spleen, congenital
- 759.1 Anomalies of adrenal gland, congenital
- 759.2 Anomalies of other endocrine glands, congenital
- 759.3 Situs inversus
- 759.4 Conjoined twins
- 759.5 Tuberous sclerosis
- 759.6 Other congenital hamartoses, not elsewhere classified
  - Cowden syndrome
- 759.7 Multiple congenital anomalies, so described
- 759.8 Other specified congenital anomalies
  - 759.81 Prader-Willi syndrome
  - 759.82 Marfan syndrome
  - 759.83 Fragile X syndrome
  - 759.89 Other specified congenital anomalies
- 759.9 Congenital anomaly, unspecified

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v t e Congenital malformations and deformations of ears
Size	Macrotia Microtia Anotia
Position	Low-set ears
Other	Accessory auricle Mondini dysplasia

v t e Congenital malformations and deformations of face and neck
Face	jaw: Otocephaly mouth: Macrostomia Microstomia lip: Macrocheilia Microcheilia chin: Microgenia multiple/other: Hallermann–Streiff syndrome Branchial cleft cyst
Neck	Webbed neck
Ungrouped	Preauricular sinus and cyst

v t e Congenital diaphragm and abdominal wall defects, abdominopelvic cavity
Thoracic diaphragm	Hernia Congenital diaphragmatic hernia Bochdalek hernia
Abdominal wall	Omphalocele Gastroschisis Prune belly syndrome

v t e Congenital malformations and deformations of skin appendages
Nail disease	Anonychia Leukonychia Pachyonychia congenita/Onychauxis Koilonychia
Hair disease	hypotrichosis/abnormalities: keratin disease Monilethrix IBIDS syndrome Sabinas brittle hair syndrome Pili annulati Pili torti Uncombable hair syndrome Björnstad syndrome Giant axonal neuropathy with curly hair hypertrichosis: Zimmermann–Laband syndrome

v t e Congenital malformations and deformations of the breast
Breast	Amastia Polymastia Micromastia Symmastia Tuberous breasts
Nipple	Athelia Polythelia

v t e Lymphatic disease: organ and vessel diseases
Thymus	Abscess Hyperplasia Hypoplasia DiGeorge syndrome Ectopic thymus Thymoma Thymic carcinoma
Spleen	Asplenia Asplenia with cardiovascular anomalies Accessory spleen Polysplenia Wandering spleen Splenomegaly Banti's syndrome Splenic infarction Splenic tumor
Lymph node	Lymphadenopathy Generalized lymphadenopathy Castleman's disease Intranodal palisaded myofibroblastoma Kikuchi disease Tonsils see Template:Respiratory pathology
Lymphatic vessels	Lymphangitis Lymphangiectasia Lymphedema Primary lymphedema Congenital lymphedema Lymphedema praecox Lymphedema tarda Lymphedema–distichiasis syndrome Milroy's disease Secondary lymphedema Bullous lymphedema Factitial lymphedema Postinflammatory lymphedema Postmastectomy lymphangiosarcoma Waldmann disease

v t e Congenital endocrine disorders
Pituitary	Congenital hypopituitarism
Thyroid	Thyroid disease Persistent thyroglossal duct Thyroglossal cyst Congenital hypothyroidism Thyroid dysgenesis Thyroid dyshormonogenesis Pendred syndrome
Parathyroid	Congenital absence of parathyroid
Adrenal	Absent adrenal gland

v t e Twin conditions
Zygosity	Twin
Monochorionic twins	Twin-to-twin transfusion syndrome Twin reversed arterial perfusion Monoamniotic twins
Conjoined twins	Parasitic twin Craniopagus parasiticus Fetus in fetu
Other	Vanishing twin Chimerism Mixed twins

v t e Phakomatosis
Angiomatosis	Sturge–Weber syndrome Von Hippel–Lindau disease
Hamartoma	Tuberous sclerosis Hypothalamic hamartoma (Pallister–Hall syndrome) Multiple hamartoma syndrome Proteus syndrome Cowden syndrome Bannayan–Riley–Ruvalcaba syndrome Lhermitte–Duclos disease
Neurofibromatosis	Type I Type II
Other	Abdallat–Davis–Farrage syndrome Ataxia telangiectasia Incontinentia pigmenti Peutz–Jeghers syndrome Encephalocraniocutaneous lipomatosis

v t e Congenital abnormality syndromes
Craniofacial	Acrocephalosyndactylia Apert syndrome Carpenter syndrome Pfeiffer syndrome Saethre–Chotzen syndrome Sakati–Nyhan–Tisdale syndrome Bonnet–Dechaume–Blanc syndrome Other Baller–Gerold syndrome Cyclopia Goldenhar syndrome Möbius syndrome
Short stature	1q21.1 deletion syndrome Aarskog–Scott syndrome Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome Robinow syndrome Silver–Russell syndrome Seckel syndrome Smith–Lemli–Opitz syndrome Snyder–Robinson syndrome Turner syndrome
Limbs	Adducted thumb syndrome Holt–Oram syndrome Klippel–Trénaunay–Weber syndrome Nail–patella syndrome Rubinstein–Taybi syndrome Gastrulation/mesoderm: Caudal regression syndrome Ectromelia Sirenomelia VACTERL association
Overgrowth syndromes	Beckwith–Wiedemann syndrome Proteus syndrome Perlman syndrome Sotos syndrome Weaver syndrome Klippel–Trénaunay–Weber syndrome Benign symmetric lipomatosis Bannayan–Riley–Ruvalcaba syndrome Neurofibromatosis type I
Laurence–Moon–Bardet–Biedl	Bardet–Biedl syndrome Laurence–Moon syndrome
Combined/other, known locus	2 (Feingold syndrome) 3 (Zimmermann–Laband syndrome) 4/13 (Fraser syndrome) 8 (Branchio-oto-renal syndrome, CHARGE syndrome) 12 (Keutel syndrome, Timothy syndrome) 15 (Marfan syndrome) 19 (Donohue syndrome) Multiple Fryns syndrome