
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