
2013 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 2013 version of ICD-9-CM 759.9.
- More recent version(s) of ICD-9-CM 759.9: 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