2012 ICD-9-CM Diagnosis Code 759.9
Congenital anomaly, unspecified
- Short description: Congenital anomaly NOS.
- ICD-9-CM 759.9 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 759.9 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2012 version of ICD-9-CM 759.9.
- More recent version(s) of ICD-9-CM 759.9: 2013 2014 2015.
Convert to ICD-10-CM:
759.9 converts directly to:
- 2015/16 ICD-10-CM Q89.9 Congenital malformation, unspecified
Approximate Synonyms
- Congenital anomaly
- Congenital deformity
- Lymphatic malformation
ICD-9-CM Volume 2 Index entries containing back-references to
759.9:
- Abnormal, abnormality, abnormalities - see also Anomaly
- anatomical relationship NEC 759.9
- development, developmental NEC 759.9
- Anomaly, anomalous (congenital) (unspecified type) 759.9
- abdomen 759.9
- Alder (-Reilly) (leukocyte granulation) 288.2
- aorticopulmonary septum 745.0
- apertures, diaphragm 756.6
- aqueduct of Sylvius 742.3
- with spina bifida (see also Spina bifida) 741.0
- arm 755.50
- reduction (see also Deformity, reduction, upper limb) 755.20
- arteriovenous (congenital) (peripheral) NEC 747.60
- artery (see also Anomaly, peripheral vascular system) NEC 747.60
- arytenoepiglottic folds 748.3
- atrial
- atrioventricular
- atrium - see Anomaly, atrial
- auricle
- autosomes, autosomal NEC 758.5
- back 759.9
- band
- biliary duct or passage 751.60
- bladder (neck) (sphincter) (trigone) 753.9
- blood vessel 747.9
- artery - see Anomaly, artery
- peripheral vascular - see Anomaly, peripheral vascular system
- vein - see Anomaly, vein
- bulbus cordis 745.9
- persistent (in left ventricle) 745.8
- capillary NEC (see also Anomaly, peripheral vascular system) 747.60
- cardiovascular system 746.9
- complicating pregnancy, childbirth, or puerperium 648.5
- caruncle, lacrimal, lachrymal 743.9
- cerebral - see also Anomaly, brain vessels 747.81
- cervix (uterus) 752.40
- with doubling of vagina and uterus 752.2
- in pregnancy or childbirth 654.6
- affecting fetus or newborn 763.89
- causing obstructed labor 660.2
- affecting fetus or newborn 763.1
- Chédiak-Higashi (-Steinbrinck) (congenital gigantism of peroxidase granules) 288.2
- chromosomes, chromosomal 758.9
- communication
- coronary artery 746.85
- left ventricle with right atrium 745.4
- connection
- renal vessels with kidney 747.62
- total pulmonary venous 747.41
- coronary
- cranium - see Anomaly, skull
- dental arch relationship 524.20
- angle's class I 524.21
- angle's class II 524.22
- angle's class III 524.23
- articulation
- disto-occlusion 524.22
- excessive horizontal overlap 524.26
- interarch distance (excessive) (inadequate) 524.28
- mesio-occlusion 524.23
- neutro-occlusion 524.21
- open
- anterior occlusal relationship 524.24
- posterior occlusal relationship 524.25
- specified NEC 524.29
- Descemet's membrane 743.9
- development
- diaphragm, diaphragmatic (apertures) NEC 756.6
- digestive organ(s) or system 751.9
- distribution, coronary artery 746.85
- ductus
- ear 744.3
- causing impairment of hearing 744.00
- external 744.3
- causing impairment of hearing 744.02
- specified type NEC 744.29
- inner (causing impairment of hearing) 744.05
- middle, except ossicles (causing impairment of hearing) 744.03
- ossicles 744.04
- prominent auricle 744.29
- specified type NEC 744.29
- with hearing impairment 744.09
- Eisenmenger's (ventricular septal defect) 745.4
- endocrine gland NEC 759.2
- fixation, intestine 751.4
- flexion (joint) 755.9
- hip or thigh (see also Dislocation, hip, congenital) 754.30
- foramen
- forehead (see also Anomaly, skull) 756.0
- frontal bone (see also Anomaly, skull) 756.0
- gastrointestinal tract 751.9
- genitalia, genital organ(s) or system
- granulation or granulocyte, genetic 288.2
- hard tissue formation in pulp 522.3
- head (see also Anomaly, skull) 756.0
- hourglass
- hypersegmentation of neutrophils, hereditary 288.2
- ileocecal (coil) (valve) 751.5
- interarch distance (excessive) (inadequate) 524.28
- intervertebral cartilage or disc 756.10
- intestine (large) (small) 751.5
- jaw-cranial base relationship 524.10
- joint 755.9
- hip
- dislocation (see also Dislocation, hip, congenital) 754.30
- predislocation (see also Subluxation, congenital, hip) 754.32
- preluxation (see also Subluxation, congenital, hip) 754.32
- subluxation (see also Subluxation, congenital, hip) 754.32
- lumbosacral 756.10
- multiple arthrogryposis 754.89
- sacroiliac 755.69
- kidney(s) (calyx) (pelvis) 753.9
- Klippel-Feil (brevicollis) 756.16
- labyrinth, membranous (causing impairment of hearing) 744.05
- lacrimal
- Langdon Down (mongolism) 758.0
- larynx, laryngeal (muscle) 748.3
- leg (lower) (upper) 755.60
- reduction NEC (see also Deformity, reduction, lower limb) 755.30
- leukocytes, genetic 288.2
- granulation (constitutional) 288.2
- limb, except reduction deformity 755.8
- lower 755.60
- reduction deformity (see also Deformity, reduction, lower limb) 755.30
- specified type NEC 755.69
- upper 755.50
- reduction deformity (see also Deformity, reduction, upper limb) 755.20
- specified type NEC 755.59
- lumbosacral (joint) (region) 756.10
- lung (fissure) (lobe) NEC 748.60
- lymphatic system 759.9
- maxilla 524.90
- meningeal bands or folds, constriction of 742.8
- meningocele (see also Spina bifida) 741.9
- middle ear, except ossicles (causing impairment of hearing) 744.03
- mitral (leaflets) (valve) 746.9
- musculoskeletal system, except limbs 756.9
- nasal sinus or septum 748.1
- nose, nasal (bone) (cartilage) (septum) (sinus) 748.1
- omphalomesenteric duct 751.0
- opening, pulmonary veins 747.49
- optic
- opticociliary vessels 743.9
- organ
- of Corti (causing impairment of hearing) 744.05
- or site 759.9
- origin
- both great arteries from same ventricle 745.11
- coronary artery 746.85
- innominate artery 747.69
- left coronary artery from pulmonary artery 746.85
- pulmonary artery 747.39
- renal vessels 747.62
- subclavian artery (left) (right) 747.21
- palate (hard) (soft) 750.9
- cleft (see also Cleft, palate) 749.00
- pelger-Huët (hereditary hyposegmentation) 288.2
- peripheral vascular system NEC 747.60
- rotation - see also Malrotation
- hip or thigh (see also Subluxation, congenital, hip) 754.32
- saddle
- salivary gland or duct 750.9
- seminal duct or tract 752.9
- septum
- heart - see Anomaly, heart, septum
- nasal 748.1
- sex chromosomes NEC (see also Anomaly, chromosomes) 758.81
- shoulder (girdle) (joint) 755.50
- site NEC 759.9
- skeleton generalized NEC 756.50
- specified type NEC
- adrenal (gland) 759.1
- alimentary tract (complete) (partial) 751.8
- ankle 755.69
- anus, anal (canal) 751.5
- aorta, aortic 747.29
- appendix 751.5
- arm 755.59
- artery (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
- auditory canal 744.29
- causing impairment of hearing 744.02
- bile duct or passage 751.69
- bladder 753.8
- bone(s) 756.9
- brain 742.4
- breast 757.6
- broad ligament 752.19
- bronchus 748.3
- canal of Nuck 752.89
- cardiac septal closure 745.8
- carpus 755.59
- cartilaginous 756.9
- cecum 751.5
- cervix 752.49
- chest (wall) 756.3
- chin 744.89
- ciliary body 743.46
- circulatory system 747.89
- clavicle 755.51
- clitoris 752.49
- coccyx 756.19
- colon 751.5
- common duct 751.69
- connective tissue 756.89
- cricoid cartilage 748.3
- cystic duct 751.69
- diaphragm 756.6
- digestive organ(s) or tract 751.8
- duodenum 751.5
- ear 744.29
- auricle 744.29
- causing impairment of hearing 744.02
- causing impairment of hearing 744.09
- inner (causing impairment of hearing) 744.05
- middle, except ossicles 744.03
- ejaculatory duct 752.89
- endocrine 759.2
- epiglottis 748.3
- esophagus 750.4
- Eustachian tube 744.24
- eye 743.8
- face 744.89
- fallopian tube 752.19
- fascia 756.89
- femur 755.69
- fibula 755.69
- finger 755.59
- foot 755.67
- fovea centralis 743.55
- gallbladder 751.69
- Gartner's duct 752.89
- gastrointestinal tract 751.8
- genitalia, genital organ(s)
- genitourinary tract NEC 752.89
- glottis 748.3
- hair 757.4
- hand 755.59
- heart 746.89
- hepatic duct 751.69
- hydatid of Morgagni 752.89
- hymen 752.49
- integument 757.8
- intestine (large) (small) 751.5
- iris 743.46
- jejunum 751.5
- joint 755.8
- kidney 753.3
- knee 755.64
- labium (majus) (minus) 752.49
- labyrinth, membranous 744.05
- larynx 748.3
- leg 755.69
- lens 743.39
- limb, except reduction deformity 755.8
- lower 755.69
- reduction deformity (see also Deformity, reduction, lower limb) 755.30
- upper 755.59
- reduction deformity (see also Deformity, reduction, upper limb) 755.20
- lip 750.26
- liver 751.69
- lung (fissure) (lobe) 748.69
- meatus urinarius 753.8
- metacarpus 755.59
- mouth 750.26
- Müllerian
- muscle 756.89
- musculoskeletal system, except limbs 756.9
- nail 757.5
- neck 744.89
- nerve 742.8
- nervous system 742.8
- nipple 757.6
- nose 748.1
- organ NEC 759.89
- osseous meatus (ear) 744.03
- ovary 752.0
- oviduct 752.19
- pancreas 751.7
- parathyroid 759.2
- patella 755.64
- pelvic girdle 755.69
- penis 752.69
- pericardium 746.89
- peripheral vascular system NEC (see also Anomaly, peripheral vascular system) 747.60
- pharynx 750.29
- pituitary 759.2
- prostate 752.89
- radius 755.59
- rectum 751.5
- respiratory system 748.8
- rib 756.3
- round ligament 752.89
- sacrum 756.19
- salivary duct or gland 750.26
- scapula 755.59
- sclera 743.47
- scrotum 752.89
- seminal duct or tract 752.89
- shoulder girdle 755.59
- site NEC 759.89
- skin 757.39
- skull (bone(s)) 756.0
- specified organ or site NEC 759.89
- spermatic cord 752.89
- spinal cord 742.59
- spine 756.19
- spleen 759.0
- sternum 756.3
- stomach 750.7
- tarsus 755.67
- tendon 756.89
- testis 752.89
- thorax (wall) 756.3
- thymus 759.2
- thyroid (gland) 759.2
- tibia 755.69
- toe 755.66
- tongue 750.19
- trachea (cartilage) 748.3
- ulna 755.59
- urachus 753.7
- ureter 753.4
- urethra 753.8
- urinary tract 753.8
- uterus (Müllerian) 752.39
- uvula 750.26
- vagina 752.49
- vascular NEC (see also Anomaly, peripheral vascular system) 747.60
- vas deferens 752.89
- vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
- vena cava (inferior) (superior) 747.49
- vertebra 756.19
- vulva 752.49
- talipes - see Talipes
- tarsus 755.67
- with complete absence of distal elements 755.31
- termination
- thigh 755.60
- flexion (see also Subluxation, congenital, hip) 754.32
- tricuspid (leaflet) (valve) 746.9
- trunk 759.9
- Uhl's (hypoplasia of myocardium, right ventricle) 746.84
- umbilicus 759.9
- union, trachea with larynx 748.3
- unspecified site 759.9
- urinary tract or system (any part, except urachus) 753.9
- uterus 752.39
- with only one functioning horn 752.33
- in pregnancy or childbirth 654.0
- affecting fetus or newborn 763.89
- causing obstructed labor 660.2
- affecting fetus or newborn 763.1
- vascular NEC (see also Anomaly, peripheral vascular system) 747.60
- vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
- vena cava (inferior) (superior) 747.40
- venous - see Anomaly, vein
- venous return (pulmonary) 747.49
- ventricle, ventricular (heart) 746.9
- vesicourethral orifice 753.9
- vessels NEC (see also Anomaly, peripheral vascular system) 747.60
- Defect, defective 759.9
- 3-beta-hydroxysteroid dehydrogenase 255.2
- abdominal wall, congenital 756.70
- aorticopulmonary septum 745.0
- atrial septal (ostium secundum type) 745.5
- atrioventricular
- bilirubin excretion 277.4
- biosynthesis, testicular androgen 257.2
- butanol-insoluble iodide 246.1
- chromosome - see Anomaly, chromosome
- circulation (acquired) 459.9
- clotting NEC (see also Defect, coagulation) 286.9
- coagulation (factor) (see also Deficiency, coagulation factor) 286.9
- with
- abortion - see Abortion, by type, with hemorrhage
- ectopic pregnancy (see also categories 634-638) 639.1
- molar pregnancy (see also categories 630-632) 639.1
- acquired (any) 286.7
- antepartum or intrapartum 641.3
- affecting fetus or newborn 762.1
- causing hemorrhage of pregnancy or delivery 641.3
- complicating pregnancy, childbirth, or puerperium 649.3
- due to
- newborn, transient 776.3
- postpartum 666.3
- specified type NEC 286.9
- conduction (heart) 426.9
- bone (see also Deafness, conductive) 389.00
- congenital, organ or site NEC - see also Anomaly
- circulation 747.9
- Descemet's membrane 743.9
- diaphragm 756.6
- ectodermal 757.9
- esophagus 750.9
- pulmonic cusps - see Anomaly, heart valve
- respiratory system 748.9
- dentin (hereditary) 520.5
- Descemet's membrane (congenital) 743.9
- developmental - see also Anomaly, by site
- cauda equina 742.59
- left ventricle 746.9
- with atresia or hypoplasia of aortic orifice or valve, with hypoplasia of ascending aorta 746.7
- in hypoplastic left heart syndrome 746.7
- testis 752.9
- vessel 747.9
- diaphragm
- with elevation, eventration, or hernia - see Hernia, diaphragm
- congenital 756.6
- with elevation, eventration, or hernia 756.6
- gross (with elevation, eventration, or hernia) 756.6
- ectodermal, congenital 757.9
- Eisenmenger's (ventricular septal defect) 745.4
- esophagus, congenital 750.9
- extensor retinaculum 728.9
- fibrin polymerization (see also Defect, coagulation) 286.3
- filling
- gene, carrier (suspected) of V83.89
- glaucomatous, without elevated tension 365.89
- Hageman (factor) (see also Defect, coagulation) 286.3
- hearing (see also Deafness) 389.9
- interauricular septal 745.5
- interventricular septal 745.4
- with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2
- acquired 429.71
- in tetralogy of Fallot 745.2
- iodotyrosine dehalogenase 246.1
- mental (see also Disability, intellectual) 319
- ostium
- placental blood supply - see Placenta, insufficiency
- platelet (qualitative) 287.1
- pulmonic cusps, congenital 746.00
- respiratory system, congenital 748.9
- septal (closure) (heart) NEC 745.9
- speech NEC 784.59
- developmental 315.39
- late effect of cerebrovascular disease - see Late effect(s) (of) cerebrovascular disease, speech and language deficit
- secondary to organic lesion 784.59
- Taussig-Bing (transposition, aorta and overriding pulmonary artery) 745.11
- thyroid hormone synthesis 246.1
- vascular (acquired) (local) 459.9
- congenital (peripheral) NEC 747.60
- ventricular septal 745.4
- with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle 745.2
- acquired 429.71
- atrioventricular canal type 745.69
- between infundibulum and anterior portion 745.4
- in tetralogy of Fallot 745.2
- isolated anterior 745.4
- wedge, teeth (abrasion) 521.20
- Deformity 738.9
- abdomen, congenital 759.9
- congenital, organ or site not listed (see also Anomaly) 759.9
- lymphatic system, congenital 759.9
- trunk (acquired) 738.3
- congenital 759.9
- Embryopathia NEC 759.9
- Malformation (congenital) - see also Anomaly
- umbilicus 759.9