2009 ICD-9-CM Diagnosis Code 759.89 : Other specified congenital anomalies

Free ICD-9-CM Diagnosis Codes > 2009 > Congential Anomalies 740-759 > Other and unspecified congenital anomalies 759.* >

2009 ICD-9-CM Diagnosis Code 759.89

Other specified congenital anomalies

759.83

759.9

759.89 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 759.89: 2010

Diagnosis Definition(s) Click to expand

Also applicable to/known as Click to expand

ICD-9-CM Volume 2 Index Entries That Refer To 759.89 Click to expand

Abrachiocephalia

759.89

Abrachiocephalus

759.89

Absence (organ or part) (complete or partial)

heart (congenital) 759.89
- acquired - see Status, organ replacement
organ
- or site
  - congenital NEC 759.89

Acardia

759.89

Arcadiacus amorphus

759.89

Acardius

759.89

Acephalobrachia

759.89

Acephalocardia

759.89

Acephalocardius

759.89

Acephalochiria

759.89

Acephalochirus

759.89

Acephalogaster

759.89

Acephalostomus

759.89

Acephalothorax

759.89

Alagille syndrome

759.89

Alport's syndrome (hereditary hematurianephropathy-deafness)

759.89

Anomaly, anomalous (congenital) (unspecified type) 759.9

multiple NEC 759.7
- specified type NEC 759.89
organ
- or site 759.9
  - specified type NEC 759.89
specified type NEC
- organ NEC 759.89
  - of Corti 744.05
- site NEC 759.89
- specified organ or site NEC 759.89

Atresia, atretic (congenital)

759.89

alimentary organ or tract NEC 751.8
- lower 751.2
- upper 750.8
ani, anus, anal (canal) 751.2
aorta 747.22
- with hypoplasia of ascending aorta and defective development of left ventricle (with mitral valve atresia) 746.7
- arch 747.11
- ring 747.21
aortic (orifice) (valve) 746.89
- arch 747.11
aqueduct of Sylvius 742.3
- with spina bifida (see also Spina bifida) 741.0
artery NEC (see also Atresia, blood vessel) 747.60
- cerebral 747.81
- coronary 746.85
- eye 743.58
- pulmonary 747.3
- umbilical 747.5
auditory canal (external) 744.02
bile, biliary duct (common) or passage 751.61
- acquired (see also Obstruction, biliary) 576.2
bladder (neck) 753.6
blood vessel (peripheral) NEC 747.60
- cerebral 747.81
- gastrointestinal 747.61
- lower limb 747.64
- pulmonary artery 747.3
- renal 747.62
- spinal 747.82
- upper limb 747.63
bronchus 748.3
canal, ear 744.02
cardiac
- valve 746.89
  - aortic 746.89
  - mitral 746.89
  - pulmonary 746.01
  - tricuspid 746.1
cecum 751.2
cervix (acquired) 622.4
- congenital 752.49
- in pregnancy or childbirth 654.6
  - affecting fetus or newborn 763.89
  - causing obstructed labor 660.2
    - affecting fetus or newborn 763.1
choana 748.0
colon 751.2
cystic duct 751.61
- acquired 575.8
  - with obstruction (see also Obstruction, gallbladder) 575.2
digestive organs NEC 751.8
duodenum 751.1
ear canal 744.02
ejaculatory duct 752.89
epiglottis 748.3
esophagus 750.3
Eustachian tube 744.24
fallopian tube (acquired) 628.2
- congenital 752.19
follicular cyst 620.0
foramen of
- Luschka 742.3
  - with spina bifida (see also Spina bifida) 741.0
- Magendie 742.3
  - with spina bifida (see also Spina bifida) 741.0
gallbladder 751.69
genital organ
- external
  - female 752.49
  - male NEC 752.89
    - penis 752.69
- internal
  - female 752.89
  - male 752.89
glottis 748.3
gullet 750.3
heart
- valve NEC 746.89
  - aortic 746.89
  - mitral 746.89
  - pulmonary 746.01
  - tricuspid 746.1
hymen 752.42
- acquired 623.3
- postinfective 623.3
ileum 751.1
intestine (small) 751.1
- large 751.2
iris, filtration angle (see also Buphthalmia) 743.20
jejunum 751.1
kidney 753.3
lacrimal, apparatus 743.65
- acquired - see Stenosis, lacrimal
larynx 748.3
ligament, broad 752.19
lung 748.5
meatus urinarius 753.6
mitral valve 746.89
- with atresia or hypoplasia of aortic orifice or valve, with hypoplasia of ascending aorta and defective development of left ventricle 746.7
nares (anterior) (posterior) 748.0
nasolacrimal duct 743.65
nasopharynx 748.8
nose, nostril 748.0
- acquired 738.0
organ or site NEC - see Anomaly, specified type NEC
osseous meatus (ear) 744.03
oviduct (acquired) 628.2
- congenital 752.19
parotid duct 750.23
- acquired 527.8
pulmonary (artery) 747.3
- valve 746.01
- vein 747.49
pulmonic 746.01
pupil 743.46
rectum 751.2
salivary duct or gland 750.23
- acquired 527.8
sublingual duct 750.23
- acquired 527.8
submaxillary duct or gland 750.23
- acquired 527.8
trachea 748.3
tricuspid valve 746.1
ureter 753.29
ureteropelvic junction 753.21
ureterovesical orifice 753.22
urethra (valvular) 753.6
urinary tract NEC 753.29
uterus 752.3
- acquired 621.8
vagina (acquired) 623.2
- congenital 752.49
- postgonococcal (old) 098.2
- postinfectional 623.2
- senile 623.2
vascular NEC (see also Atresia, blood vessel) 747.60
- cerebral 747.81
vas deferens 752.89
vein NEC (see also Atresia, blood vessel) 747.60
- cardiac 746.89
- great 747.49
- portal 747.49
- pulmonary 747.49
vena cava (inferior) (superior) 747.49
vesicourethral orifice 753.6
vulva 752.49
- acquired 624.8

Barth syndrome

759.89

Beckwith (-Wiedemann) syndrome

759.89

Biedl-Bardet syndrome

759.89

Biemond's syndrome (obesity, polydactyly, and mental retardation)

759.89

Birt-Hogg-Dube syndrome

759.89

Brachman-de Lange syndrome (Amsterdam dwarf, mental retardation, and brachycephaly)

759.89

Brachymorphism and ectopia lentis

759.89

Bruck-de Lange disease or syndrome (Amsterdam dwart, mental retardation, and brachycephaly)

759.89

Carpenter's syndrome

759.89

Cerebrohepatorenal syndrome

759.89

CGF (congenital generalized fibromatosis)

759.89

CHARGE association (syndrome)

759.89

Cockayne's disease or syndrome (microcephaly and dwarfism)

759.89

Congenital - see also condition

generalized fibromatosis (CGF) 759.89

Cornelia de Lange's syndrome (Amsterdam dwarf, mental retardation, and brachycephaly)

759.89

Cyclencephaly

759.89

Cyclopia, cyclops

759.89

Cyllosoma

759.89

Cyst (mucus) (retention) (serous) (simple)

congenital NEC 759.89
- adrenal glands 759.1
- epiglottis 748.3
- esophagus 750.4
- fallopian tube 752.11
- kidney 753.10
  - multiple 753.19
  - single 753.11
- larynx 748.3
- liver 751.62
- lung 748.4
- mediastinum 748.8
- ovary 752.0
- oviduct 752.11
- pancreas 751.7
- periurethral (tissue) 753.8
- prepuce NEC 752.69
  - penis 752.69
- sublingual 750.26
- submaxillary gland 750.26
- thymus (gland) 759.2
- tongue 750.19
- ureterovesical orifice 753.4
- vulva 752.41
umbilicus 759.89

Deformity 738.9

multiple, congenital NEC 759.7
- specified type NEC 759.89

de Lange's syndrome (Amsterdam dwarf, mental retardation, and brachycephaly)

759.89

Disease, diseased - see also Syndrome

Bruck-de Lange (Amsterdam dwarf, mental retardation, and brachycephaly) 759.89
Cockayne's (microcephaly and dwarfism) 759.89
Kok 759.89
polycystic (congenital) 759.89
- kidney or renal 753.12
  - adult type (APKD) 753.13
  - autosomal dominant 753.13
  - autosomal recessive 753.14
  - childhood type (CPKD) 753.14
  - infantile type 753.14
- liver or hepatic 751.62
- lung or pulmonary 518.89
  - congenital 748.4
- ovary, ovaries 256.4
- spleen 759.0
Startle 759.89

Dwarf, dwarfism 259.4

Amsterdam 759.89
bird-headed 759.89
Russell's (uterine dwarfism and craniofacial dysostosis) 759.89

Dyscraniopyophalangy

759.89

Dysostosis

orodigitofacial 759.89

Dysplasia - see also Anomaly

craniocarpotarsal 759.89
linguofacialis 759.89
oculodentodigital 759.89

Ectopic, ectopia (congenital)

759.89

abdominal viscera 751.8
- due to defect in anterior abdominal wall 756.79
ACTH syndrome 255.0
adrenal gland 759.1
anus 751.5
auricular beats 427.61
beats 427.60
bladder 753.5
bone and cartilage in lung 748.69
brain 742.4
breast tissue 757.6
cardiac 746.87
cerebral 742.4
cordis 746.87
endometrium 617.9
gallbladder 751.69
gastric mucosa 750.7
gestation - see Pregnancy, ectopic
heart 746.87
hormone secretion NEC 259.3
hyperparathyroidism 259.3
kidney (crossed) (intrathoracic) (pelvis) 753.3
- in pregnancy or childbirth 654.4
  - causing obstructed labor 660.2
lens 743.37
lentis 743.37
mole - see Pregnancy, ectopic
organ or site NEC - see Malposition, congenital
ovary 752.0
pancreas, pancreatic tissue 751.7
pregnancy - see Pregnancy, ectopic
pupil 364.75
renal 753.3
sebaceous glands of mouth 750.26
secretion
- ACTH 255.0
- adrenal hormone 259.3
- adrenalin 259.3
- adrenocorticotropin 255.0
- antidiuretic hormone (ADH) 259.3
- epinephrine 259.3
- hormone NEC 259.3
- norepinephrine 259.3
- pituitary (posterior) 259.3
spleen 759.0
testis 752.51
thyroid 759.2
ureter 753.4
ventricular beats 427.69
vesicae 753.5

Fibromatosis 728.79

congenital generalized (CGF) 759.89

Finnish type nephrosis (congenital)

759.89

Fistula (sinus) 686.9

umbilical 759.89

Fraser's syndrome

759.89

Freeman-Sheldon syndrome

759.89

Gillespie's syndrome (dysplasia oculodentodigitalis)

759.89

Gorlin-Chaudhry-Moss syndrome

759.89

Hemihypertrophy (congenital)

759.89

cranial 756.0

Hyperekplexia

759.89

Hyperexplexia

759.89

Hypoplasia, hypoplasis

759.89

adrenal (gland) 759.1
alimentary tract 751.8
- lower 751.2
- upper 750.8
anus, anal (canal) 751.2
aorta 747.22
aortic
- arch (tubular) 747.10
- orifice or valve with hypoplasia of ascending aorta and defective development of left ventricle (with mitral valve atresia) 746.7
appendix 751.2
areola 757.6
arm (see also Absence, arm, congenital) 755.20
artery (congenital) (peripheral) 747.60
- brain 747.81
- cerebral 747.81
- coronary 746.85
- gastrointestinal 747.61
- lower limb 747.64
- pulmonary 747.3
- renal 747.62
- retinal 743.58
- specified NEC 747.69
- spinal 747.82
- umbilical 747.5
- upper limb 747.63
auditory canal 744.29
- causing impairment of hearing 744.02
biliary duct (common) or passage 751.61
bladder 753.8
bone NEC 756.9
- face 756.0
- malar 756.0
- mandible 524.04
  - alveolar 524.74
- marrow 284.9
  - acquired (secondary) 284.89
  - congenital 284.09
  - idiopathic 284.9
- maxilla 524.03
  - alveolar 524.73
- skull (see also Hypoplasia, skull) 756.0
brain 742.1
- gyri 742.2
- specified part 742.2
breast (areola) 611.82
bronchus (tree) 748.3
cardiac 746.89
- valve - see Hypoplasia, heart, valve
- vein 746.89
carpus (see also Absence, carpal, congenital) 755.28
cartilaginous 756.9
cecum 751.2
cementum 520.4
- hereditary 520.5
cephalic 742.1
cerebellum 742.2
cervix (uteri) 752.49
chin 524.06
clavicle 755.51
coccyx 756.19
colon 751.2
corpus callosum 742.2
cricoid cartilage 748.3
dermal, focal (Goltz) 757.39
digestive organ(s) or tract NEC 751.8
- lower 751.2
- upper 750.8
ear 744.29
- auricle 744.23
- lobe 744.29
- middle, except ossicles 744.03
  - ossicles 744.04
- ossicles 744.04
enamel of teeth (neonatal) (postnatal) (prenatal) 520.4
- hereditary 520.5
endocrine (gland) NEC 759.2
endometrium 621.8
epididymis 752.89
epiglottis 748.3
erythroid, congenital 284.01
erythropoietic, chronic acquired 284.81
esophagus 750.3
Eustachian tube 744.24
eye (see also Microphthalmos) 743.10
- lid 743.62
face 744.89
- bone(s) 756.0
fallopian tube 752.19
femur (see also Absence, femur, congenital) 755.34
fibula (see also Absence, fibula, congenital) 755.37
finger (see also Absence, finger, congenital) 755.29
focal dermal 757.39
foot 755.31
gallbladder 751.69
genitalia, genital organ(s)
- female 752.89
  - external 752.49
  - internal NEC 752.89
- in adiposogenital dystrophy 253.8
- male 752.89
  - penis 752.69
glottis 748.3
hair 757.4
hand 755.21
heart 746.89
- left (complex) (syndrome) 746.7
- valve NEC 746.89
  - pulmonary 746.01
humerus (see also Absence, humerus, congenital) 755.24
hymen 752.49
intestine (small) 751.1
- large 751.2
iris 743.46
jaw 524.09
kidney(s) 753.0
labium (majus) (minus) 752.49
labyrinth, membranous 744.05
lacrimal duct (apparatus) 743.65
larynx 748.3
leg (see also Absence, limb, congenital, lower) 755.30
limb 755.4
- lower (see also Absence, limb, congenital, lower) 755.30
- upper (see also Absence, limb, congenital, upper) 755.20
liver 751.69
lung (lobe) 748.5
mammary (areolar) 611.82
mandibular 524.04
- alveolar 524.74
- unilateral condylar 526.89
maxillary 524.03
- alveolar 524.73
medullary 284.9
megakaryocytic 287.30
metacarpus (see also Absence, metacarpal, congenital) 755.28
metatarsus (see also Absence, metatarsal, congenital) 755.38
muscle 756.89
- eye 743.69
myocardium (congenital) (Uhl's anomaly) 746.84
nail(s) 757.5
nasolacrimal duct 743.65
nervous system NEC 742.8
neural 742.8
nose, nasal 748.1
ophthalmic (see also Microphthalmos) 743.10
optic nerve 377.43
organ
- of Corti 744.05
- or site NEC - see Anomaly, by site
osseous meatus (ear) 744.03
ovary 752.0
oviduct 752.19
pancreas 751.7
parathyroid (gland) 759.2
parotid gland 750.26
patella 755.64
pelvis, pelvic girdle 755.69
penis 752.69
peripheral vascular system (congenital) NEC 747.60
- gastrointestinal 747.61
- lower limb 747.64
- renal 747.62
- specified NEC 747.69
- spinal 747.82
- upper limb 747.63
pituitary (gland) 759.2
pulmonary 748.5
- arteriovenous 747.3
- artery 747.3
- valve 746.01
punctum lacrimale 743.65
radioulnar (see also Absence, radius, congenital, with ulna) 755.25
radius (see also Absence, radius, congenital) 755.26
rectum 751.2
respiratory system NEC 748.9
rib 756.3
sacrum 756.19
scapula 755.59
shoulder girdle 755.59
skin 757.39
skull (bone) 756.0
- with
  - anencephalus 740.0
  - encephalocele 742.0
  - hydrocephalus 742.3
    - with spina bifida (see also Spina bifida) 741.0
  - microcephalus 742.1
spinal (cord) (ventral horn cell) 742.59
- vessel 747.82
spine 756.19
spleen 759.0
sternum 756.3
tarsus (see also Absence, tarsal, congenital) 755.38
testis, testicle 752.89
thymus (gland) 279.11
thyroid (gland) 243
- cartilage 748.3
tibiofibular (see also Absence, tibia, congenital, with fibula) 755.35
toe (see also Absence, toe, congenital) 755.39
tongue 750.16
trachea (cartilage) (rings) 748.3
Turner's (tooth) 520.4
ulna (see also Absence, ulna, congenital) 755.27
umbilical artery 747.5
ureter 753.29
uterus 752.3
vagina 752.49
vascular (peripheral) NEC (see also Hypoplasia, peripheral vascular system) 747.60
- brain 747.81
vein(s) (peripheral) NEC (see also Hypoplasia, peripheral vascular system) 747.60
- brain 747.81
- cardiac 746.89
- great 747.49
- portal 747.49
- pulmonary 747.49
vena cava (inferior) (superior) 747.49
vertebra 756.19
vulva 752.49
zonule (ciliary) 743.39
zygoma 738.12

Joubert syndrome

759.89

Kabuki syndrome

759.89

Klippel-Trenaunay syndrome

759.89

Laurence-Moon-Biedl syndrome (obesity, polydactyly, and mental retardation)

759.89

Marchesani (-Weill) syndrome (brachymorphism and ectopia lentis)

759.89

Meyer-Schwickerath and Weyers syndrome (dysplasia oculodentodigitalis)

759.89

Microphthalmos (congenital) 743.10

syndrome 759.89

Mieten's syndrome

759.89

Mohr's syndrome (types I and II)

759.89

Myofibromatosis

infantile 759.89

Negri bodies 071

Neill-Dingwall syndrome (microcephaly and dwarfism) 759.89

Nephritis, nephritic (albuminuric) (azotemic) (congenital) (degenerative) (diffuse) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic) 583.9

hereditary (Alport's syndrome) 759.89

Nephrosis, nephrotic (Epstein's) (syndrome) 581.9

Finnish type (congenital) 759.89

Nevus (M8720/0) - see also Neoplasm, skin, benign

flammeus 757.32
- osteohypertrophic 759.89
osteohypertrophic, flammeus 759.89

Orodigitofacial dysostosis

759.89

Papillon-Léage and Psaume syndrome (orodigitofacial dysostosis)

759.89

Persistence, persistent (congenital)

759.89

anal membrane 751.2
arteria stapedia 744.04
atrioventricular canal 745.69
bloody ejaculate 792.2
branchial cleft 744.41
bulbus cordis in left ventricle 745.8
canal of Cloquet 743.51
capsule (opaque) 743.51
cilioretinal artery or vein 743.51
cloaca 751.5
communication - see Fistula, congenital
convolutions
- aortic arch 747.21
- fallopian tube 752.19
- oviduct 752.19
- uterine tube 752.19
double aortic arch 747.21
ductus
- arteriosus 747.0
- Botalli 747.0
fetal
- circulation 747.83
- form of cervix (uteri) 752.49
- hemoglobin (hereditary) ("Swiss variety") 282.7
- pulmonary hypertension 747.83
foramen
- Botalli 745.5
- ovale 745.5
Gartner's duct 752.41
hemoglobin, fetal (hereditary) (HPFH) 282.7
hyaloid
- artery (generally incomplete) 743.51
- system 743.51
hymen (tag)
- in pregnancy or childbirth 654.8
  - causing obstructed labor 660.2
lanugo 757.4
left
- posterior cardinal vein 747.49
- root with right arch of aorta 747.21
- superior vena cava 747.49
Meckel's diverticulum 751.0
mesonephric duct 752.89
- fallopian tube 752.11
mucosal disease (middle ear) (with posterior or superior marginal perforation of ear drum) 382.2
nail(s), anomalous 757.5
occiput, anterior or posterior 660.3
- fetus or newborn 763.1
omphalomesenteric duct 751.0
organ or site NEC - see Anomaly, specified type NEC
ostium
- atrioventriculare commune 745.69
- primum 745.61
- secundum 745.5
ovarian rests in fallopian tube 752.19
pancreatic tissue in intestinal tract 751.5
primary (deciduous)
- teeth 520.6
- vitreous hyperplasia 743.51
pulmonary hypertension 747.83
pupillary membrane 743.46
- iris 743.46
- Rhesus (Rh) titer 999.7
right aortic arch 747.21
sinus
- urogenitalis 752.89
- venosus with imperfect incorporation in right auricle 747.49
thymus (gland) 254.8
- hyperplasia 254.0
thyroglossal duct 759.2
thyrolingual duct 759.2
truncus arteriosus or communis 745.0
tunica vasculosa lentis 743.39
umbilical sinus 753.7
urachus 753.7
vegetative state 780.03
vitelline duct 751.0
wolffian duct 752.89

Podencephalus

759.89

Polycystic (congenital) (disease)

759.89

degeneration, kidney - see Polycystic, kidney
kidney (congenital) 753.12
- adult type (APKD) 753.13
- autosomal dominant 753.13
- autosomal recessive 753.14
- childhood type (CPKD) 753.14
- infantile type 753.14
liver 751.62
lung 518.89
- congenital 748.4
ovary, ovaries 256.4
spleen 759.0

Pseudo-Turner's syndrome

759.89

Rubinstein-Taybi's syndrome (brachydactylia, short stature and mental retardation)

759.89

Rud's syndrome (mental deficiency, epilepsy, and infantilism)

759.89

Russell's dwarf (uterine dwarfism and craniofacial dysostosis)

759.89

Russell (-Silver) syndrome (congenital hemihypertrophy and short stature)

759.89

Seborrhea, seborrheic 706.3

nigricans 759.89

Seckel's syndrome

759.89

Sick 799.9

cilia syndrome 759.89

Silver's syndrome (congenital hemihypertrophy and short stature

759.89

Sirenomelia

759.89

Smith-Lemli-Opitz syndrome (cerebrohepatorenal syndrome)

759.89

Stickler syndrome

759.89

Stiff-baby

759.89

Sympus

759.89

Syndrome - see also Disease

Alagille 759.89
Alport's (hereditary hematuria-nephropathy-deafness) 759.89
Angelman 759.89
Bardet-Biedl (obesity, polydactyly, and mental retardation) 759.89
Barth 759.89
Beckwith (-Wiedemann) 759.89
Biedl-Bardet (obesity, polydactyly, and mental retardation) 759.89
Biemond's (obesity, polydactyly, and mental retardation) 759.89
Birt-Hogg-Dube 759.89
Borjeson-Forssman-Lehmann 759.89
Brachman-de Lange (Amsterdam dwarf, mental retardation, and brachycephaly) 759.89
Carpenter's 759.89
cerebrohepatorenal 759.89
CHARGE association 759.89
Cockayne's (microencephaly and dwarfism) 759.89
Coffin-Lowry 759.89
congenital
- affecting more than one system 759.7
  - specified type NEC 759.89
- muscular hypertrophy-cerebral 759.89
de Lange's (Amsterdam dwarf, mental retardation, and brachycephaly) (Cornelia) 759.89
Fraser's 759.89
Freeman-Sheldon 759.89
Gillespie's (dysplasia oculodentodigitalis) 759.89
Gorlin-Chaudhry-Moss 759.89
inverted Marfan's 759.89
Joubert 759.89
Kabuki 759.89
Klippel-Trenaunay 759.89
Laurence-Moon (-Bardet)-Biedl (obesity, polydactyly, and mental retardation) 759.89
Marchesani (-Weill) (brachymorphism and ectopia lentis) 759.89
Menkes' 759.89
- glutamic acid 759.89
- maple syrup (urine) disease 270.3
Meyer-Schwickerath and Weyers (dysplasia oculodentodigitalis) 759.89
microphthalmos (congenital) 759.89
Mieten's 759.89
Mohr's (types I and II) 759.89
Neill Dingwall (microencephaly and dwarfism) 759.89
Noonan's 759.89
oral-facial-digital 759.89
ordigitofacial 759.89
otopalatodigital 759.89
Papillon-Léage and Psaume (orodigitofacial dysostosis) 759.89
pseudo-Turner's 759.89
Rubinstein-Taybi's (brachydactylia, short stature, and mental retardation) 759.89
Rud's (mental deficiency, epilepsy, and infantilism) 759.89
Russell (-Silver) (congenital hemihypertrophy and short stature) 759.89
Seckel's 759.89
sick
- cilia 759.89
Silver's (congenital hemihypertrophy and short stature) 759.89
Smith-Lemli-Opitz (cerebrohepatorenal syndrome) 759.89
spherophakia-brachymorphia 759.89
Stickler 759.89
stiff-baby 759.89
Taybi's (otopalatodigital) 759.89
Ullrich-Feichtiger 759.89
VATER 759.89
Weill-Marchesani (brachymorphism and ectopia lentis) 759.89
"whistling face" (craniocarpotarsal dystrophy) 759.89

Synophthalmus

759.89

Taybi's syndrome (otopalatodigital)

759.89

Teratencephalus

759.89

Thoracogastroschisis (congenital)

759.89

Ullrich-Feichtiger syndrome

759.89

VATER syndrome

759.89

Weill-Marchesani syndrome (brachymorphism and ectopia lentis)

759.89

"Whistling face" syndrome (craniocarpotarsal dystrophy)

759.89

New to the world of medical coding? ICD-9-CM codes are used throughout the healthcare industry to describe diseases, injuries, symptoms and conditions. CPT codes are used to describe medical and surgical services performed by healthcare providers. ICD-9-CM codes and CPT codes are inherently related, as the diagnosis (ICD-9-CM code) must support the procedure (CPT code). All Medicare claims require a valid ICD-9-CM diagnosis code and a CPT procedure code in order to be reimbursed. Turn to ICD9Data.com as your free searchable ICD-9-CM code lookup source... and for everything related to diagnosis coding.