2011 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 2011 version of ICD-9-CM 759.9.
- More recent version(s) of ICD-9-CM 759.9: 2012 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 747.3
- 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