| ICDCode | Description |
| 740. | Anencephalus and similar anomalies |
| 740.0 | Anencephalus; anencephaly |
| 740.1 | Craniorachischisis |
| 740.2 | Iniencephaly |
| 741. | Spina bifida; neural tube defects |
| 741.0 | Spina bifida with hydrocephalus |
| 741.00 | Spin Bif W Hydroceph Nos |
| 741.01 | Spin Bif W Hydrceph-cerv |
| 741.02 | Spin Bif W Hydrceph-dors |
| 741.03 | Spin Bif W Hydrceph-lumb |
| 741.9 | Spina bifida without mention of hydrocephalus |
| 741.90 | Spina bifida with hydrocephalus without hydrocephalus unspecified |
| 741.91 | Spina Bifida-cerv |
| 741.92 | Spina Bifida-dorsal |
| 741.93 | Spina Bifida-lumbar |
| 742. | Other congenital anomalies of nervous system |
| 742.0 | Encephalocele |
| 742.1 | Microcephalus; microencephaly; microcephaly |
| 742.2 | Reduction deformities of brain; holoprosencephaly |
| 742.3 | Hydrocephalus; congenital hydrocephalus; Dandy-Walker malformation |
| 742.4 | Other specified anomalies of brain (congenital cyst, macroencephaly, macrogyria, megalencephaly) |
| 742.5 | Other specified anomalies of spinal cord |
| 742.51 | Diastematomyelia |
| 742.53 | Hydromyelia |
| 742.59 | Anomalies of the spinal cord (myelodysplastic syndromes) |
| 742.8 | Other specified anomalies of the nervous system |
| 742.9 | Nervous System Anom Nos |
| 743. | Congenital anomalies of eye |
| 743.0 | Anophthalmos |
| 743.00 | Clinic Anophthalmos Nos |
| 743.03 | Congen Cystic Eyeball |
| 743.06 | Cryptophthalmos |
| 743.1 | Microphthalmos |
| 743.10 | Microphthalmos Nos |
| 743.11 | Simple Microphthalmos |
| 743.12 | Microphth W Oth Eye Anom |
| 743.2 | Buphthalmos (congenital glaucoma, hydrophthalmos) |
| 743.20 | Buphthalmos Nos |
| 743.21 | Simple Buphthalmos |
| 743.22 | Buphthal W Oth Eye Anom |
| 743.3 | Congenital cataract (infantile cataract); congenital cataract and lens anomalies |
| 743.30 | Congenital Cataract Nos |
| 743.31 | Capsular Cataract |
| 743.32 | Cortical/zonular Catarac |
| 743.33 | Nuclear Cataract |
| 743.34 | Cong Tot/subtot Cataract |
| 743.35 | Congenital Aphakia |
| 743.36 | Anomalies Of Lens Shape |
| 743.37 | Congenital Ectopic Lens |
| 743.39 | Cong Catar/lens Anom Nec |
| 743.4 | Coloboma and other anomalies of anterior segment |
| 743.41 | Anom Corneal Size/shape |
| 743.42 | Cong Cornea Opac Aff Vis |
| 743.43 | Cong Corneal Opacit Nec |
| 743.44 | Anom Anter Chamber-eye |
| 743.45 | Aniridia |
| 743.46 | Anom Iris & Cil Body Nec |
| 743.47 | Anomalies Of Sclera |
| 743.48 | Mult Anom Anter Seg-eye |
| 743.49 | Anom Anter Seg Nec-eye |
| 743.5 | Congenital anomalies of posterior segment |
| 743.51 | Vitreous Anomalies |
| 743.52 | Fundus Coloboma |
| 743.53 | Cong Chorioretinal Degen |
| 743.54 | Cong Fold/cyst Post Eye |
| 743.55 | Cong Macular Change-eye |
| 743.56 | Cong Retinal Changes Nec |
| 743.57 | Specific anomalies of optic disc |
| 743.58 | Vascular Anom Post Eye |
| 743.59 | Post Segmnt Anom Nec-eye |
| 743.6 | Congenital anomalies of eyelids, lacrimal system, and orbit |
| 743.61 | Congenital Ptosis |
| 743.62 | Congenital Eyelid Deform |
| 743.63 | Spec Anom Of Eyelid Nec |
| 743.64 | Spec Lacrimal Gland Anom |
| 743.65 | Spec Lacrimal Pass Anom |
| 743.66 | Spec Anomaly Of Orbit |
| 743.69 | Anom Eyelid/lacr/orb Nec |
| 743.8 | Other specified anomalies of the eye |
| 743.9 | Eye Anomaly Nos |
| 744. | Congenital anomalies of ear |
| 744.0 | Anomalies of ear causing impairment of hearing |
| 744.00 | Ear Anom Nos/impair Hear |
| 744.01 | Cong Absence Ext Ear |
| 744.02 | Other anomalies of external ear with impairment of hearing |
| 744.03 | Middle Ear Anomaly Nec |
| 744.04 | Anomalies Ear Ossicles |
| 744.05 | Anomalies Of Inner Ear |
| 744.09 | Ear Anom Nec/impair Hear |
| 744.1 | Accessory Auricle |
| 744.2 | Other specified anomalies of ear |
| 744.21 | Cong Absence Of Ear Lobe |
| 744.22 | Macrotia |
| 744.23 | Microtia; anotia |
| 744.24 | Eustachian Tube Anom Nec |
| 744.29 | Ear Anomalies Nec |
| 744.3 | Ear Anomaly Nos |
| 744.4 | Branchial cleft cyst or fistula; preauricular sinus |
| 744.41 | Branch Cleft Sinus/fistu |
| 744.42 | Branchial Cleft Cyst |
| 744.43 | Cervical Auricle |
| 744.46 | Preauricular Sinus/fistu |
| 744.47 | Preauricular Cyst |
| 744.49 | Branchial Cleft Anom Nec |
| 744.5 | Webbing Of Neck |
| 744.8 | Other specified anomalies of face and neck |
| 744.81 | Macrocheilia |
| 744.82 | Microcheilia |
| 744.83 | Macrostomia |
| 744.84 | Microstomia |
| 744.89 | Cong Face/neck Anom Nec |
| 744.9 | Cong Face/neck Anom Nos |
| 745. | Bulbus cordis anomalies and anomalies of cardiac septal closure |
| 745.0 | Common truncus anomaly; truncus arteriosus (common truncus) |
| 745.1 | Transposition of the great arteries |
| 745.10 | Compl Transpos Great Ves |
| 745.11 | Double outlet right ventricle |
| 745.12 | Correct Transpos Grt Ves |
| 745.19 | Transpos Great Vess Nec |
| 745.2 | Tetralogy of Fallot |
| 745.3 | Common Ventricle |
| 745.4 | Ventricular septal defect; Eisenmenger syndrome |
| 745.5 | Atrial septal defect (ASD); patent foramen ovale (PFO) |
| 745.6 | Endocardial cushion defects |
| 745.60 | Endocard Cushion Def Nos |
| 745.61 | Ostium primum defect (Persistent ostium primum) |
| 745.69 | Atrioventricular septal defect (AVSD); other endocardial cushion defects |
| 745.7 | Cor Biloculare |
| 745.8 | Septal Closure Anom Nec |
| 745.9 | Septal Closure Anom Nos |
| 746. | Other congenital heart anomalies; congenital heart disease |
| 746.0 | Pulmonary valve anomaly |
| 746.00 | Pulmonary Valve Anom Nos |
| 746.01 | Pulmonary atresia; pulmonary valve atresia |
| 746.02 | Pulmonary stenosis (pulmonic stenosis); congenital pulmonary valve stenosis |
| 746.09 | Pulmonary Valve Anom Nec |
| 746.1 | Tricuspid atresia; tricuspid stenosis |
| 746.2 | Ebstein anomaly |
| 746.3 | Congenital stenosis of aortic valve |
| 746.4 | Congenital insufficiency of aortic valve; congenital bicuspid aortic valve |
| 746.5 | Congenital mitral stenosis |
| 746.6 | Cong Mitral Insufficienc |
| 746.7 | Hypoplastic left heart syndrome |
| 746.71 | Hypoplastic right heart syndrome |
| 746.8 | Other specified congenital anomalies of heart; congenital heart disease |
| 746.81 | Cong Subaortic Stenosis |
| 746.82 | Cor Triatriatum |
| 746.83 | Infundib Pulmon Stenosis |
| 746.84 | Obstruct Heart Anom Nec |
| 746.85 | Coronary Artery Anomaly |
| 746.86 | Congenital heart block; complete or incomplete atrioventricular block (AV block) |
| 746.87 | Malposition of heart; dextrocardia |
| 746.89 | Other specified congenital anomalies of heart |
| 746.9 | Unspecified anomaly of heart |
| 747. | Other congenital anomalies of circulatory system |
| 747.0 | Patent ductus arteriosus |
| 747.1 | Coarctation of the aorta; aortic coarctation |
| 747.10 | Coarctation of the aorta |
| 747.11 | Aortic arch interruption |
| 747.2 | Other anomalies of the aorta |
| 747.20 | Cong Anom Of Aorta Nos |
| 747.21 | Anomalies Of Aortic Arch |
| 747.22 | Aortic Atresia/stenosis |
| 747.29 | Cong Anom Of Aorta Nec |
| 747.3 | Congenital anomalies of pulmonary artery |
| 747.4 | Anomalies of great veins |
| 747.40 | Great Vein Anomaly Nos |
| 747.41 | Tot Anom Pulm Ven Connec |
| 747.42 | Part Anom Pulm Ven Conn |
| 747.49 | Anomalous pulmonary venous connection; pulmonary venous anomaly; Scimitar syndrome |
| 747.5 | Absence or hypoplasia of umbilical artery (single umbilical artery) |
| 747.6 | Other congenital anomalies of peripheral vascular system |
| 747.60 | Anomaly of the peripheral vascular system, unspecified site |
| 747.61 | Gstrontest Vesl Anomaly |
| 747.62 | Renal Vessel Anomaly |
| 747.63 | Upr Limb Vessel Anomaly |
| 747.64 | Lwr Limb Vessel Anomaly |
| 747.69 | Oth Spcf Prph Vscl Anoml |
| 747.8 | Other specified congenital anomalies of circulatory system |
| 747.81 | Arteriovenous malformation (AVM); cavernous malformation; anomalies of cerebrovascular system |
| 747.82 | Spinal Vessel Anomaly |
| 747.83 | Persistent Fetal Circ |
| 747.89 | Circulatory Anomaly Nec |
| 747.9 | Circulatory Anomaly Nos |
| 748. | Congenital anomalies of respiratory system |
| 748.0 | Choanal atresia |
| 748.1 | Other anomalies of nose |
| 748.2 | Laryngeal Web |
| 748.3 | Other congenital anomalies of larynx; laryngomalacia |
| 748.4 | Congenital Cystic Lung |
| 748.5 | Agenesis, hypoplasia, and dysplasia of lung |
| 748.6 | Other anomalies of lung |
| 748.60 | Lung Anomaly Nos |
| 748.61 | Congen Bronchiectasis |
| 748.69 | Lung Anomaly Nec |
| 748.8 | Respiratory Anomaly Nec |
| 748.9 | Respiratory Anomaly Nos |
| 749. | Cleft palate and cleft lip |
| 749.0 | Cleft palate |
| 749.00 | Cleft Palate Nos |
| 749.01 | Unilat Cleft Palate-comp |
| 749.02 | Unilat Cleft Palate-inc |
| 749.03 | Bilat Cleft Palate-compl |
| 749.04 | Bilat Cleft Palate-inc |
| 749.1 | Cleft lip |
| 749.10 | Cleft Lip Nos |
| 749.11 | Unilat Cleft Lip-compl |
| 749.12 | Unilat Cleft Lip-imcompl |
| 749.13 | Bilat Cleft Lip-complete |
| 749.14 | Bilat Cleft Lip-incompl |
| 749.2 | Cleft palate with cleft lip |
| 749.20 | Cleft Palate & Lip Nos |
| 749.21 | Unil Cleft Palat/lip-com |
| 749.22 | Unil Cleft Palat/lip-inc |
| 749.23 | Bilat Clft Palat/lip-com |
| 749.24 | Bilat Clft Palat/lip-inc |
| 749.25 | Cleft Palate & Lip Nec |
| 750. | Other congenital anomalies of upper alimentary tract |
| 750.0 | Ankyloglossia (tongue tie) |
| 750.1 | Other anomalies of tongue |
| 750.10 | Tongue Anomaly Nos |
| 750.11 | Aglossia |
| 750.12 | Cong Adhesions Of Tongue |
| 750.13 | Cong Fissure Of Tongue |
| 750.15 | Cong Macroglossia |
| 750.16 | Microglossia |
| 750.19 | Tongue Anomaly Nec |
| 750.2 | Other specified anomalies of mouth and pharynx |
| 750.21 | Salivary Gland Absence |
| 750.22 | Accessory Salivary Gland |
| 750.23 | Cong Atresia, Saliv Duct |
| 750.24 | Cong Salivary Fistula |
| 750.25 | Congenital Lip Fistula |
| 750.26 | Mouth Anomaly Nec |
| 750.27 | Diverticulum Of Pharynx |
| 750.29 | Pharyngeal Anomaly Nec |
| 750.3 | Tracheoesophageal fistula, esophageal atresia, and stenosis |
| 750.4 | Esophageal Anomaly Nec |
| 750.5 | Pyloric stenosis; infantile hypertrophic pyloric stenosis |
| 750.6 | Congenital Hiatus Hernia |
| 750.7 | Gastric Anomaly Nec |
| 750.8 | Upper Gi Anomaly Nec |
| 750.9 | Upper Gi Anomaly Nos |
| 751. | Other congenital anomalies of digestive system |
| 751.0 | Meckel's diverticulum |
| 751.1 | Intestinal atresia; duodenal atresia; duodenal stenosis; choanal atresia; colonic atresia; anorectal malformation |
| 751.2 | Atresia and stenosis of large intestine, rectum, and anal canal |
| 751.3 | Hirschsprung's disease and other congenital functional disorders of the colon (congenital megacolon) |
| 751.4 | Anomalies of intestinal fixation |
| 751.5 | Other congenital anomalies of intestine |
| 751.6 | Anomalies of gallbladder, bile ducts, and liver |
| 751.60 | Biliary & Liver Anom Nos |
| 751.61 | Biliary atresia |
| 751.62 | Polycystic liver disease; autosomal-dominant polycystic liver disease (ADPLD) |
| 751.69 | Other congenital anomalies of gallbladder, bile ducts, and liver |
| 751.7 | Pancreas Anomalies |
| 751.8 | Other specified anomalies of digestive system |
| 751.9 | Anom Digestive Syst Nos |
| 752. | Congenital anomalies of genital organs |
| 752.0 | Anomalies Of Ovaries |
| 752.1 | Congenital anomalies of fallopian tubes and broad ligaments |
| 752.10 | Tubal/broad Lig Anom Nos |
| 752.11 | Embryonic cyst of fallopian tubes and broad ligaments |
| 752.19 | Tubal/broad Lig Anom Nec |
| 752.2 | Doubling of uterus (didelphic uterus) |
| 752.3 | Uterine Anomaly Nec |
| 752.4 | Anomalies of cervix, vagina, and external female genitalia |
| 752.40 | Cervix/fem Gen Anom Nos |
| 752.41 | Embryon Cyst Fem Gen Nec |
| 752.42 | Imperforate Hymen |
| 752.49 | Other anomalies of cervix, vagina, and external female genitalia |
| 752.5 | Undescended and retractile testicle |
| 752.51 | Cryptorchidism (undescended testis) |
| 752.52 | Retractile Testis |
| 752.6 | Hypospadias and epispadias |
| 752.61 | Hypospadias (unspecified) |
| 752.62 | Epispadias |
| 752.63 | Congenital Chordee |
| 752.64 | Micropenis |
| 752.65 | Hidden Penis |
| 752.69 | Penile torsion; penile anomalies not elsewhere classified |
| 752.7 | Indeterminate sex (pseudohermaphroditism) |
| 752.8 | Other specified anomalies of genital organs |
| 752.81 | Scrotal transposition |
| 752.89 | Other specified anomalies of genital organs; unilateral absence of the vas deferens (UAVD) |
| 752.9 | Genital Organ Anom Nos |
| 753. | Congenital anomalies of urinary system |
| 753.0 | Renal agenesis; renal dysgenesis |
| 753.1 | Cystic kidney disease |
| 753.10 | Cystic kidney disease, unspecified |
| 753.11 | Congenital single renal cyst |
| 753.12 | Polycystic kidney, unspecified |
| 753.13 | Autosomal dominant polycystic kidney disease (ADPKD) |
| 753.14 | Autosomal recessive polycystic kidney disease |
| 753.15 | Renal Dysplasia |
| 753.16 | Medullary Cystic Kidney |
| 753.17 | Medullary Sponge Kidney |
| 753.19 | Unspecified anomaly of the urinary system |
| 753.2 | Obstructive defects of renal pelvis and ureter |
| 753.20 | Obs Dfct Ren Plv&urt Nos |
| 753.21 | Congenital obstruction of ureteropelvic junction; ureteropelvic junction obstruction |
| 753.22 | Cong Obst Ureteroves Jnc |
| 753.23 | Congenital Ureterocele |
| 753.29 | Obst Def Ren Plv&urt Nec |
| 753.3 | Other specified anomalies of kidney |
| 753.4 | Ureteral Anomaly Nec |
| 753.5 | Exstrophy of urinary bladder; bladder exstrophy |
| 753.6 | Atresia and stenosis of urethra and bladder neck |
| 753.7 | Anomalies Of Urachus |
| 753.8 | Other specified anomalies of bladder and urethra |
| 753.9 | Urinary Anomaly Nos |
| 754. | Certain congenital musculoskeletal deformities; intoeing |
| 754.0 | Cong Skull/face/jaw Def |
| 754.1 | Congenital musculoskeletal deformities of sternocleidomastoid muscle |
| 754.2 | Cong Postural Deformity |
| 754.3 | Hip dysplasia; congenital hip dysplasia (developmental dislocation of hip); hip dislocation at birth |
| 754.30 | Cong Hip Disloc, Unilat |
| 754.31 | Congen Hip Disloc, Bilat |
| 754.32 | Cong Hip Sublux, Unilat |
| 754.33 | Cong Hip Sublux, Bilat |
| 754.35 | Cong Hip Disloc W Sublux |
| 754.4 | Congenital genu recurvatum and bowing of long bones of leg |
| 754.40 | Cong Genu Recurvatum |
| 754.41 | Cong Knee Dislocation |
| 754.42 | Congen Bowing Of Femur |
| 754.43 | Cong Bowing Tibia/fibula |
| 754.44 | Cong Bowing Leg Nos |
| 754.5 | Congenital varus deformities of feet |
| 754.50 | Talipes Varus |
| 754.51 | Clubfoot (Talipes Equinovarus) |
| 754.52 | Metatarsus Primus Varus |
| 754.53 | Metatarsus Varus |
| 754.59 | Cong Varus Foot Def Nec |
| 754.6 | Valgus deformities of feet |
| 754.60 | Talipes Valgus |
| 754.61 | Congenital pes planus; flat foot (pes planus) |
| 754.62 | Talipes Calcaneovalgus |
| 754.69 | Cong Valgus Foot Def Nec |
| 754.7 | Other deformities of feet |
| 754.70 | Talipes Nos |
| 754.71 | Talipes Cavus |
| 754.79 | Cong Foot Deform Nec |
| 754.8 | Other specified nonteratogenic anomalies |
| 754.81 | Pectus excavatum |
| 754.82 | Pectus Carinatum |
| 754.89 | Other specified nonteratogenic anomalies |
| 755. | Other congenital anomalies of limbs |
| 755.0 | Polydactyly |
| 755.00 | Polydactyly Nos |
| 755.01 | Polydactyly, Fingers |
| 755.02 | Polydactyly, Toes |
| 755.1 | Syndactyly |
| 755.10 | Syndactyly, Multiple/nos |
| 755.11 | Syndactyl Fing-no Fusion |
| 755.12 | Syndactyly; polysyndactyly |
| 755.13 | Syndactyl Toe-no Fusion |
| 755.14 | Syndactyl Toe W Fusion |
| 755.2 | Reduction deformities of upper limb |
| 755.20 | Reduc Deform Up Limb Nos |
| 755.21 | Transverse Defic Arm |
| 755.22 | Longitud Defic Arm Nec |
| 755.23 | Combin Longit Defic Arm |
| 755.24 | Longitudin Defic Humerus |
| 755.25 | Longitud Defic Radioulna |
| 755.26 | Longitud Defic Radius |
| 755.27 | Longitudinal Defic Ulna |
| 755.28 | Longitudinal Defic Hand |
| 755.29 | Longitud Defic Phalanges |
| 755.3 | Reduction deformities of lower limb; anomalies of lower limb; limb deficiency; limb defect |
| 755.30 | Reduction Deform Leg Nos |
| 755.31 | Transverse Defic Leg |
| 755.32 | Longitudin Defic Leg Nec |
| 755.33 | Comb Longitudin Def Leg |
| 755.34 | Longitudinal Defic Femur |
| 755.35 | Tibiofibula Longit Defic |
| 755.36 | Longitudinal Defic Tibia |
| 755.37 | Longitudin Defic Fibula |
| 755.38 | Longitudinal Defic Foot |
| 755.39 | Longitud Defic Phalanges |
| 755.4 | Reduction deformities, unspecified limb |
| 755.5 | Other anomalies of upper limb, including shoulder girdle |
| 755.50 | Upper Limb Anomaly Nos |
| 755.51 | Cong Deformity-clavicle |
| 755.52 | Cong Elevation-scapula |
| 755.53 | Radioulnar Synostosis |
| 755.54 | Madelungs Deformity |
| 755.55 | Acrocephalosyndactyly; Apert's syndrome |
| 755.56 | Accessory Carpal Bones |
| 755.57 | Macrodactylia (fingers) |
| 755.58 | Congenital Cleft Hand |
| 755.59 | Upper Limb Anomaly Nec |
| 755.6 | Other congenital anomalies of lower limb |
| 755.60 | Lower Limb Anomaly Nos |
| 755.61 | Congenital Coxa Valga |
| 755.62 | Congenital Coxa Vara |
| 755.63 | Other congenital deformities of hip (joint) |
| 755.64 | Cong Knee Deformity |
| 755.65 | Macrodactylia Of Toes |
| 755.66 | Anomalies Of Toes Nec |
| 755.67 | Anomalies Of Foot Nec |
| 755.69 | Lower Limb Anomaly Nec |
| 755.8 | Congen Limb Anomaly Nec |
| 755.9 | Congen Limb Anomaly Nos |
| 756. | Other congenital musculoskeletal anomalies |
| 756.0 | Anomalies of skull and face bones (craniosynostosis, Treacher Collins syndrome, plagiocephaly, microsomia, Rubinstein-Tabyi syndrome; Crouzon syndrome, Saethre-Chotzen syndrome, and others) |
| 756.1 | Congenital anomalies of spine |
| 756.10 | Anomaly Of Spine Nos |
| 756.11 | Spondylolysis |
| 756.12 | Spondylolisthesis |
| 756.13 | Cong Absence Of Vertebra |
| 756.14 | Hemivertebra |
| 756.15 | Congen Fusion Of Spine |
| 756.16 | Klippel-Feil syndrome |
| 756.17 | Spina Bifida Occulta |
| 756.19 | Anomaly Of Spine Nec |
| 756.2 | Cervical Rib |
| 756.3 | Rib & Sternum Anomal Nec |
| 756.4 | Achondroplasia; Chondrodystrophy; Chondrodysplasia |
| 756.5 | Osteodystrophies |
| 756.50 | Skeletal dysplasia; osteodystrophy; osteochondrodysplasia |
| 756.51 | Osteogenesis imperfecta |
| 756.52 | Osteopetrosis |
| 756.53 | Osteopoikilosis |
| 756.54 | Polyostotic Fibros Dyspl |
| 756.55 | Chondroectoderm Dysplas |
| 756.56 | Mult Epiphyseal Dysplas |
| 756.59 | Osteodystrophy Nec |
| 756.6 | Congenital anomalies of diaphragm |
| 756.7 | Congenital anomalies of abdominal wall |
| 756.70 | Congn Anoml Abd Wall Nos |
| 756.71 | Prune belly syndrome |
| 756.72 | Omphalocele |
| 756.73 | Gastroschisis |
| 756.79 | Congn Anoml Abd Wall Nec |
| 756.8 | Other specified anomalies of muscle, tendon, fascia, and connective tissue |
| 756.81 | Absence Of Muscle/tendon |
| 756.82 | Accessory Muscle |
| 756.83 | Ehlers-Danlos syndrome |
| 756.89 | Other specified anomalies of muscle, tendon, fascia; Poland syndrome; nail-patella syndrome |
| 756.9 | Other and unspecified anomalies of musculoskeletal system |
| 756.90 | Waardenburg syndrome |
| 757. | Congenital anomalies of integument |
| 757.0 | Hereditary Edema Of Legs |
| 757.1 | Ichthyosis; ichthyosis congenita |
| 757.2 | Dermatoglyphic Anomalies |
| 757.3 | Other specified anomalies of skin |
| 757.31 | Congenital ectodermal dysplasia |
| 757.32 | Port-Wine Stain; Strawberry Hemangioma; Hamartoma; Birthmark |
| 757.33 | Congenital pigmentary anomalies of skin (poikiloderma, urticaria pigmentosa, mastocytosis, and xeroderma pigmentosum) |
| 757.39 | Other congenital anomalies of the integument; epidermolysis bullosa |
| 757.4 | Hair Anomalies Nec |
| 757.5 | Nail Anomalies Nec |
| 757.6 | Breast Anomalies Nec |
| 757.8 | Oth Integument Anomalies |
| 757.9 | Integument Anomaly Nos |
| 758. | Chromosomal anomalies |
| 758.0 | Down syndrome (trisomy 21) |
| 758.1 | Patau syndrome (Trisomy 13) |
| 758.2 | Edwards' syndrome (trisomy 18) |
| 758.3 | Autosomal deletion syndromes; cri du chat syndrome |
| 758.31 | Cri-du-chat syndrome |
| 758.32 | DiGeorge syndrome; velocardiofacial syndrome |
| 758.33 | Other microdeletions |
| 758.39 | Other autosomal deletions |
| 758.4 | Balanced autosomal translocation in normal individual |
| 758.5 | Other conditions due to autosomal anomalies |
| 758.6 | Gonadal dysgenesis; Turner syndrome (45,X); XO syndrome |
| 758.7 | Klinefelter syndrome (47,XXY) |
| 758.8 | Other conditions due to sex chromosome anomalies |
| 758.81 | Trisomy X; triple X syndrome (47,XXX); XYY male syndrome (47,XYY); 48,XXXY karyotype; 48,XXYY karyotype; 49,XXXXY karyotype
|
| 758.89 | Other conditions due to chromosome anomalies; triploidy; diploidy |
| 758.9 | Conditions due to anomaly of unspecified chromosome |
| 759. | Other and unspecified congenital anomalies |
| 759.0 | Anomalies Of Spleen |
| 759.1 | Adrenal Gland Anomaly |
| 759.2 | Ectopic thymus; endocrine anomaly not elsewhere classified |
| 759.3 | Primary Ciliary Dyskinesia; Situs inversus |
| 759.4 | Conjoined twins; Siamese twins |
| 759.5 | Tuberous sclerosis |
| 759.6 | Von Hippel-Lindau disease; Sturge-Weber syndrome; Peutz-Jeghers syndrome; hamartoses not elsewhere classified |
| 759.7 | Multiple congenital anomalies |
| 759.8 | Other congenital anomalies |
| 759.81 | Prader-Willi syndrome |
| 759.82 | Marfan syndrome |
| 759.83 | Fragile X syndrome |
| 759.88 | Barth Syndrome |
| 759.89 | Congenital Malformation Syndromes (Smith-Lemli-Opitz Syndrome, Noonan Syndrome, Beckwith-Wiedemann Syndrome, VATER Syndrome (VACTERL Association), Klippel-Trenaunay Syndrome, Williams Syndrome, Alagille Syndrome, Alport Syndrome, Barth Syndrome, Angelman Syndrome, and Others) |
| 759.9 | Congenital Anomaly Nos |
| 759.90 | Cornelia de Lange syndrome |