Other congenital anomalies of upper alimentary tract

750       Other congenital anomalies of upper alimentary tract     (ICD 9 CM Codes)

Excludes:    dentofacial anomalies (524.0-524.9)

750.0    Tongue tie

Ankyloglossia

750.1    Other anomalies of tongue

750.10  Anomaly of tongue, unspecified

750.11  Aglossia

750.12  Congenital adhesions of tongue

750.13  Fissure of tongue

Bifid tongue

Double tongue

750.15  Macroglossia

Congenital hypertrophy of tongue

750.16  Microglossia

Hypoplasia of tongue

750.19  Other

750.2    Other specified anomalies of mouth and pharynx

750.21  Absence of salivary gland

750.22  Accessory salivary gland

750.23  Atresia, salivary gland

Imperforate salivary duct

750.24  Congenital fistula of salivary gland

750.25  Congenital fistula of lip

Congenital (mucus) lip pits

750.26  Other specified anomalies of mouth

Absence of uvula

750.27  Diverticulum of pharynx

Pharyngeal pouch

750.29  Other specified anomalies of pharynx

Imperforate pharynx

750.3    Tracheoesophageal fistula, esophageal atresia and stenosis

Absent esophagus

Atresia of esophagus

Congenital:

esophageal ring

stenosis of esophagus

stricture of esophagus

Congenital fistula:

esophagobronchial

esophagotracheal

Imperforate esophagus

Webbed esophagus

750.4    Other specified anomalies of esophagus

Dilatation, congenital, of esophagus

Displacement, congenital, of esophagus

Diverticulum of esophagus

Duplication of esophagus

Giant esophagus

Esophageal pouch

Excludes: congenital hiatus hernia (750.6)

750.5    Congenital hypertrophic pyloric stenosis

Congenital or infantile:

constriction of pylorus

hypertrophy of pylorus

spasm of pylorus

stenosis of pylorus

stricture of pylorus

750.6    Congenital hiatus hernia

Displacement of cardia through esophageal hiatus

Excludes: congenital diaphragmatic hernia (756.6)

750.7    Other specified anomalies of stomach

Congenital:

cardiospasm

hourglass stomach

Displacement of stomach

Diverticulum of stomach, congenital

Duplication of stomach

Megalogastria

Microgastria

Transposition of stomach

750.8    Other specified anomalies of upper alimentary tract

750.9    Unspecified anomaly of upper alimentary tract

Congenital:

anomaly NOS of upper alimentary tract [any part, except tongue]

deformity NOS of upper alimentary tract [any part, except tongue]

751       Other congenital anomalies of digestive system         (ICD 9 CM Codes)

751.0    Meckel's diverticulum

Meckel's diverticulum (displaced) (hypertrophic)

Persistent:

omphalomesenteric duct

vitelline duct

751.1    Atresia and stenosis of small intestine

Atresia of:

duodenum

ileum

intestine NOS

Congenital:

absence of small intestine or intestine NOS

obstruction of small intestine or intestine NOS

stenosis of small intestine or intestine NOS

stricture of small intestine or intestine NOS

Imperforate jejunum

751.2    Atresia and stenosis of large intestine, rectum, and anal canal

Absence:

anus (congenital)

appendix, congenital

large intestine, congenital

rectum

Atresia of:

anus

colon

rectum

Congenital or infantile:

obstruction of large intestine

occlusion of anus

stricture of anus

Imperforate:

anus

rectum

Stricture of rectum, congenital

751.3    Hirschsprung's disease and other congenital functional disorders of colon

Aganglionosis

Congenital dilation of colon

Congenital megacolon

Macrocolon

751.4    Anomalies of intestinal fixation

Congenital adhesions:

omental, anomalous

peritoneal

Jackson's membrane

Malrotation of colon

Rotation of cecum or colon:

failure of

incomplete

insufficient

Universal mesentery

751.5    Other anomalies of intestine

Congenital diverticulum, colon

Dolichocolon

Duplication of:

anus

appendix

cecum

intestine

Ectopic anus

Megaloappendix

Megaloduodenum

Microcolon

Persistent cloaca

Transposition of:

appendix

colon

intestine

751.6    Anomalies of gallbladder, bile ducts, and liver

751.60  Unspecified anomaly of gallbladder, bile ducts, and liver

751.61  Biliary atresia

Congenital:

absence of bile duct (common) or passage

hypoplasia of bile duct (common) or passage

obstruction of bile duct (common) or passage

stricture of bile duct (common) or passage

751.62  Congenital cystic disease of liver

Congenital polycystic disease of liver

Fibrocystic disease of liver

751.69  Other anomalies of gallbladder, bile ducts, and liver

Absence of:

gallbladder, congenital

liver (lobe)

Accessory:

hepatic ducts

liver

Congenital:

choledochal cyst

hepatomegaly

Duplication of:

biliary duct

cystic duct

gallbladder

liver

Floating:

gallbladder

liver

Intrahepatic gallbladder

751.7    Anomalies of pancreas

Absence of pancreas

Accessory pancreas

Agenesis of pancreas

Annular pancreas

Ectopic pancreatic tissue

Hypoplasia of pancreas

Pancreatic heterotopia

Excludes: diabetes mellitus (249.0-249.9, 250.0-250.9)

fibrocystic disease of pancreas (277.00-277.09)

neonatal diabetes mellitus (775.1)

751.8    Other specified anomalies of digestive system

Absence (complete) (partial) of alimentary tract NOS

Duplication of digestive organs NOS

Malposition, congenital of digestive organs NOS

Excludes: congenital diaphragmatic hernia (756.6)

congenital hiatus hernia (750.6)

751.9    Unspecified anomaly of digestive system

Congenital:

anomaly NOS of digestive system NOS

deformity NOS of digestive system NOS

752       Congenital anomalies of genital organs          (ICD 9 CM Codes)

Excludes:    syndromes associated with anomalies in the number and form of chromosomes (758.0-758.9)

752.0    Anomalies of ovaries

Absence, congenital, of ovary

Accessory ovary

Ectopic ovary

Streak of ovary

752.1    Anomalies of fallopian tubes and broad ligaments

752.10  Unspecified anomaly of fallopian tubes and broad ligaments

752.11  Embryonic cyst of fallopian tubes and broad ligaments

Cyst:

epoophoron

fimbrial

parovarian

752.19  Other

Absence of fallopian tube or broad ligament

Accessory fallopian tube or broad ligament

Atresia of fallopian tube or broad ligament

752.2    Doubling of uterus

Didelphic uterus

Doubling of uterus [any degree] (associated with doubling of cervix and vagina)

752.3    Other anomalies of uterus

752.31  Agenesis of uterus

Congenital absence of uterus

752.32  Hypoplasia of uterus

752.33  Unicornuate uterus

Unicornate uterus with or without a separate uterine horn

Uterus with only one functioning horn

752.34  Bicornuate uterus

Bicornuate uterus, complete or partial

752.35  Septate uterus

Septate uterus, complete or partial

752.36  Arcuate uterus

752.39  Other anomalies of uterus

Aplasia of uterus NOS

Müllerian anomaly of the uterus, NEC

Excludes: anomaly of uterus due to exposure to diethylstilbestrol [DES] in utero (760.76)

didelphic uterus (752.2)

doubling of uterus (752.2)

752.4    Anomalies of cervix, vagina, and external female genitalia

752.40  Unspecified anomaly of cervix, vagina, and external female genitalia

752.41  Embryonic cyst of cervix, vagina, and external female genitalia

Cyst of:

canal of Nuck, congenital

Gartner's duct

vagina, embryonal

vulva, congenital

752.42  Imperforate hymen

752.43  Cervical agenesis

Cervical hypoplasia

752.44  Cervical duplication

752.45  Vaginal agenesis

Agenesis of vagina, total or partial

752.46  Transverse vaginal septum

752.47  Longitudinal vaginal septum

Longitudinal vaginal septum with or without obstruction

752.49  Other anomalies of cervix, vagina, and external female genitalia

Absence of clitoris or vulva

Agenesis of clitoris or vulva

Anomalies of cervix, NEC

Anomalies of hymen, NEC

Congenital stenosis or stricture of:

cervical canal

vagina

Müllerian anomalies of the cervix and vagina, NEC

Excludes: double vagina associated with total duplication (752.2)

752.5    Undescended and retractile testicle

752.51  Undescended testis

Cryptorchism

Ectopic testis

752.52  Retractile testis

752.6    Hypospadias and epispadias and other penile anomalies

752.61  Hypospadias

752.62  Epispadias

Anaspadias

752.63  Congenital chordee

752.64  Micropenis

752.65  Hidden penis

752.69  Other penile anomalies

752.7    Indeterminate sex and pseudohermaphroditism

Gynandrism

Hermaphroditism

Ovotestis

Pseudohermaphroditism (male) (female)

Pure gonadal dysgenesis

Excludes: androgen insensitivity (259.50-259.52)

pseudohermaphroditism:

female, with adrenocortical disorder (255.2)

male, with gonadal disorder (257.8)

with specified chromosomal anomaly (758.0-758.9)

testicular feminization syndrome (259.50-259.52)

752.8    Other specified anomalies of genital organs

Excludes: congenital hydrocele (778.6)

penile anomalies (752.61-752.69)

phimosis or paraphimosis (605)

752.81  Scrotal transposition

752.89  Other specified anomalies of genital organs

Absence of:

prostate

spermatic cord

vas deferens

Anorchism

Aplasia (congenital) of:

prostate

round ligament

testicle

Atresia of:

ejaculatory duct

vas deferens

Fusion of testes

Hypoplasia of testis

Monorchism

Polyorchism

752.9    Unspecified anomaly of genital organs

Congenital:

anomaly NOS of genital organ, NEC

deformity NOS of genital organ, NEC

753       Congenital anomalies of urinary system              (ICD 9 CM Codes)

753.0    Renal agenesis and dysgenesis

Atrophy of kidney:

congenital

infantile

Congenital absence of kidney(s)

Hypoplasia of kidney(s)

753.1    Cystic kidney disease

Excludes: acquired cyst of kidney (593.2)

753.10  Cystic kidney disease, unspecified

753.11  Congenital single renal cyst

753.12  Polycystic kidney, unspecified type

753.13  Polycystic kidney, autosomal dominant

753.14  Polycystic kidney, autosomal recessive

753.15  Renal dysplasia

753.16  Medullary cystic kidney

Nephronopthisis

753.17  Medullary sponge kidney

753.19  Other specified cystic kidney disease

Multicystic kidney

753.2    Obstructive defects of renal pelvis and ureter

753.20  Unspecified obstructive defect of renal pelvis and ureter

753.21  Congenital obstruction of ureteropelvic junction

753.22  Congenital obstruction of ureterovesical junction

Adynamic ureter

Congenital hydroureter

753.23  Congenital ureterocele

753.29  Other

753.3    Other specified anomalies of kidney

Accessory kidney

Congenital:

calculus of kidney

displaced kidney

Discoid kidney

Double kidney with double pelvis

Ectopic kidney

Fusion of kidneys

Giant kidney

Horseshoe kidney

Hyperplasia of kidney

Lobulation of kidney

Malrotation of kidney

Trifid kidney (pelvis)

753.4    Other specified anomalies of ureter

Absent ureter

Accessory ureter

Deviation of ureter

Displaced ureteric orifice

Double ureter

Ectopic ureter

Implantation, anomalous, of ureter

753.5    Exstrophy of urinary bladder

Ectopia vesicae

Extroversion of bladder

753.6    Atresia and stenosis of urethra and bladder neck

Congenital obstruction:

bladder neck

urethra

Congenital stricture of:

urethra (valvular)

urinary meatus

vesicourethral orifice

Imperforate urinary meatus

Impervious urethra

Urethral valve formation

753.7    Anomalies of urachus

Cyst (of) urachus

Fistula (of) urachus

Patent (of) urachus

Persistent umbilical sinus

753.8    Other specified anomalies of bladder and urethra

Absence, congenital of:

bladder

urethra

Accessory:

bladder

urethra

Congenital:

diverticulum of bladder

hernia of bladder

Congenital urethrorectal fistula

Congenital prolapse of:

bladder (mucosa)

urethra

Double:

urethra

urinary meatus

753.9    Unspecified anomaly of urinary system

Congenital:

anomaly NOS of urinary system [any part, except urachus]

deformity NOS  of urinary system [any part, except urachus]

754       Certain congenital musculoskeletal deformities           (ICD 9 CM Codes)

Includes:     nonteratogenic deformities which are considered to be due to intrauterine malposition and pressure

754.0    Of skull, face, and jaw

Asymmetry of face

Compression facies

Depressions in skull

Deviation of nasal septum, congenital

Dolichocephaly

Plagiocephaly

Potter's facies

Squashed or bent nose, congenital

Excludes: dentofacial anomalies (524.0-524.9)

syphilitic saddle nose (090.5)

754.1    Of sternocleidomastoid muscle

Congenital sternomastoid torticollis

Congenital wryneck

Contracture of sternocleidomastoid (muscle)

Sternomastoid tumor

754.2    Of spine

Congenital postural:

lordosis

scoliosis

754.3    Congenital dislocation of hip

754.30  Congenital dislocation of hip, unilateral

Congenital dislocation of hip NOS

754.31  Congenital dislocation of hip, bilateral

754.32  Congenital subluxation of hip, unilateral

Congenital flexion deformity, hip or thigh

Predislocation status of hip at birth

Preluxation of hip, congenital

754.33  Congenital subluxation of hip, bilateral

754.35  Congenital dislocation of one hip with subluxation of other hip

754.4    Congenital genu recurvatum and bowing of long bones of leg

754.40  Genu recurvatum

754.41  Congenital dislocation of knee (with genu recurvatum)

754.42  Congenital bowing of femur

754.43  Congenital bowing of tibia and fibula

754.44  Congenital bowing of unspecified long bones of leg

754.5    Varus deformities of feet

Excludes: acquired (736.71, 736.75, 736.79)

754.50  Talipes varus

Congenital varus deformity of foot, unspecified

Pes varus

754.51  Talipes equinovarus

Equinovarus (congenital)

754.52  Metatarsus primus varus

754.53  Metatarsus varus

754.59  Other

Talipes calcaneovarus

754.6    Valgus deformities of feet

Excludes: valgus deformity of foot (acquired) (736.79)

754.60  Talipes valgus

Congenital valgus deformity of foot, unspecified

754.61  Congenital pes planus

Congenital rocker bottom flat foot

Flat foot, congenital

Excludes: pes planus (acquired) (734)

754.62  Talipes calcaneovalgus

754.69  Other

Talipes:

equinovalgus

planovalgus

754.7    Other deformities of feet

Excludes: acquired (736.70-736.79)

754.70  Talipes, unspecified

Congenital deformity of foot NOS

754.71  Talipes cavus

Cavus foot (congenital)

754.79  Other

Asymmetric talipes

Talipes:

calcaneus

equinus

754.8    Other specified nonteratogenic anomalies

754.81  Pectus excavatum

Congenital funnel chest

754.82  Pectus carinatum

Congenital pigeon chest [breast]

754.89  Other

Club hand (congenital)

Congenital:

deformity of chest wall

dislocation of elbow

Generalized flexion contractures of lower limb joints, congenital

Spade-like hand (congenital)

755       Other congenital anomalies of limbs                   (ICD 9 CM Codes)

Excludes:    those deformities classifiable to 754.0-754.8

755.0    Polydactyly

755.00  Polydactyly, unspecified digits

Supernumerary digits

755.01  Of fingers

Accessory fingers

755.02  Of toes

Accessory toes

755.1    Syndactyly

Symphalangy

Webbing of digits

755.10  Of multiple and unspecified sites

755.11  Of fingers without fusion of bone

755.12  Of fingers with fusion of bone

755.13  Of toes without fusion of bone

755.14  Of toes with fusion of bone

755.2    Reduction deformities of upper limb

755.20  Unspecified reduction deformity of upper limb

Ectromelia NOS of upper limb

Hemimelia NOS of upper limb

Shortening of arm, congenital

755.21  Transverse deficiency of upper limb

Amelia of upper limb

Congenital absence of:

fingers, all (complete or partial)

forearm, including hand and fingers

upper limb, complete

Congenital amputation of upper limb

Transverse hemimelia of upper limb

755.22  Longitudinal deficiency of upper limb, NEC

Phocomelia NOS of upper limb

Rudimentary arm

755.23  Longitudinal deficiency, combined, involving humerus, radius, and ulna (complete or incomplete)

Congenital absence of arm and forearm (complete or incomplete) with or without metacarpal deficiency and/or phalangeal deficiency, incomplete

Phocomelia, complete, of upper limb

755.24  Longitudinal deficiency, humeral, complete or partial (with or without distal deficiencies, incomplete)

Congenital absence of humerus (with or without absence of some [but not all] distal elements)

Proximal phocomelia of upper limb

755.25  Longitudinal deficiency, radioulnar, complete or partial (with or without distal deficiencies, incomplete)

Congenital absence of radius and ulna (with or without absence of some [but not all] distal elements)

Distal phocomelia of upper limb

755.26  Longitudinal deficiency, radial, complete or partial (with or without distal deficiencies, incomplete)

Agenesis of radius

Congenital absence of radius (with or without absence of some [but not all] distal elements)

755.27  Longitudinal deficiency, ulnar, complete or partial (with or without distal deficiencies, incomplete)

Agenesis of ulna

Congenital absence of ulna (with or without absence of some [but not all] distal elements)

755.28  Longitudinal deficiency, carpals or metacarpals, complete or partial (with or without incomplete phalangeal deficiency)

755.29  Longitudinal deficiency, phalanges, complete or partial

Absence of finger, congenital

Aphalangia of upper limb, terminal, complete or partial

Excludes: terminal deficiency of all five digits (755.21)

transverse deficiency of phalanges (755.21)

755.3    Reduction deformities of lower limb

755.30  Unspecified reduction deformity of lower limb

Ectromelia NOS of lower limb

Hemimelia NOS of lower limb

Shortening of leg, congenital

755.31  Transverse deficiency of lower limb

Amelia of lower limb

Congenital absence of:

foot

leg, including foot and toes

lower limb, complete

toes, all, complete

Transverse hemimelia of lower limb

755.32  Longitudinal deficiency of lower limb, NEC

Phocomelia NOS of lower limb

755.33  Longitudinal deficiency, combined, involving femur, tibia, and fibula (complete or incomplete)

Congenital absence of thigh and (lower) leg (complete or incomplete) with or without metacarpal deficiency and/or phalangeal deficiency, incomplete

Phocomelia, complete, of lower limb

755.34  Longitudinal deficiency, femoral, complete or partial (with or without distal deficiencies, incomplete)

Congenital absence of femur (with or without absence of some [but not all] distal elements)

Proximal phocomelia of lower limb

755.35  Longitudinal deficiency, tibiofibular, complete or partial (with or without distal deficiencies, incomplete)

Congenital absence of tibia and fibula (with or without absence of some [but not all] distal elements)

Distal phocomelia of lower limb

755.36  Longitudinal deficiency, tibia, complete or partial (with or without distal deficiencies, incomplete)

Agenesis of tibia

Congenital absence of tibia (with or without absence of some [but not all] distal elements)

755.37  Longitudinal deficiency, fibular, complete or partial (with or without distal deficiencies, incomplete)

Agenesis of fibula

Congenital absence of fibula (with or without absence of some [but not all] distal elements)

755.38  Longitudinal deficiency, tarsals or metatarsals, complete or partial (with or without incomplete phalangeal deficiency)

755.39  Longitudinal deficiency, phalanges, complete or partial

Absence of toe, congenital

Aphalangia of lower limb, terminal, complete or partial

Excludes: terminal deficiency of all five digits (755.31)

transverse deficiency of phalanges (755.31)

755.4    Reduction deformities, unspecified limb

Absence, congenital (complete or partial) of limb NOS

Amelia of unspecified limb

Ectromelia of unspecified limb

Hemimelia of unspecified limb

Phocomelia of unspecified limb

755.5    Other anomalies of upper limb, including shoulder girdle

755.50  Unspecified anomaly of upper limb

755.51  Congenital deformity of clavicle

755.52  Congenital elevation of scapula

Sprengel's deformity

755.53  Radioulnar synostosis

755.54  Madelung's deformity

755.55  Acrocephalosyndactyly

Apert's syndrome

755.56  Accessory carpal bones

755.57  Macrodactylia (fingers)

755.58  Cleft hand, congenital

Lobster-claw hand

755.59  Other

Cleidocranial dysostosis

Cubitus:

valgus, congenital

varus, congenital

Excludes: club hand (congenital) (754.89)

congenital dislocation of elbow (754.89)

755.6    Other anomalies of lower limb, including pelvic girdle

755.60  Unspecified anomaly of lower limb

755.61  Coxa valga, congenital

755.62  Coxa vara, congenital

755.63  Other congenital deformity of hip (joint)

Congenital anteversion of femur (neck)

Excludes: congenital dislocation of hip (754.30-754.35)

755.64  Congenital deformity of knee (joint)

Congenital:

absence of patella

genu valgum [knock-knee]

genu varum [bowleg]

Rudimentary patella

755.65  Macrodactylia of toes

755.66  Other anomalies of toes

Congenital:

hallux valgus

hallux varus

hammer toe

755.67  Anomalies of foot, NEC

Astragaloscaphoid synostosis

Calcaneonavicular bar

Coalition of calcaneus

Talonavicular synostosis

Tarsal coalitions

755.69  Other

Congenital:

angulation of tibia

deformity (of):

ankle (joint)

sacroiliac (joint)

fusion of sacroiliac joint

755.8    Other specified anomalies of unspecified limb

755.9    Unspecified anomaly of unspecified limb

Congenital:

anomaly NOS of unspecified limb

deformity NOS of unspecified limb

Excludes: reduction deformity of unspecified limb (755.4)

756       Other congenital musculoskeletal anomalies              (ICD 9 CM Codes)

Excludes:    congenital myotonic chondrodystrophy (359.23)

those deformities classifiable to 754.0-754.8

756.0    Anomalies of skull and face bones

Absence of skull bones

Acrocephaly

Congenital deformity of forehead

Craniosynostosis

Crouzon's disease

Hypertelorism

Imperfect fusion of skull

Oxycephaly

Platybasia

Premature closure of cranial sutures

Tower skull

Trigonocephaly

Excludes: acrocephalosyndactyly [Apert's syndrome] (755.55)

dentofacial anomalies (524.0-524.9)

skull defects associated with brain anomalies, such as:

anencephalus (740.0)

encephalocele (742.0)

hydrocephalus (742.3)

microcephalus (742.1)

756.1    Anomalies of spine

756.10  Anomaly of spine, unspecified

756.11  Spondylolysis, lumbosacral region

Prespondylolisthesis (lumbosacral)

756.12  Spondylolisthesis

756.13  Absence of vertebra, congenital

756.14  Hemivertebra

756.15  Fusion of spine [vertebra], congenital

756.16  Klippel-Feil syndrome

756.17  Spina bifida occulta

Excludes: spina bifida (aperta) (741.0-741.9)

756.19  Other

Platyspondylia

Supernumerary vertebra

756.2    Cervical rib

Supernumerary rib in the cervical region

756.3    Other anomalies of ribs and sternum

Congenital absence of:

rib

sternum

Congenital:

fissure of sternum

fusion of ribs

Sternum bifidum

Excludes: nonteratogenic deformity of chest wall (754.81-754.89)

756.4    Chondrodystrophy

Achondroplasia

Chondrodystrophia (fetalis)

Dyschondroplasia

Enchondromatosis

Ollier's disease

Excludes: congenital myotonic chondrodystrophy (359.23)

lipochondrodystrophy [Hurler's syndrome] (277.5)

Morquio's disease (277.5)

756.5    Osteodystrophies

756.50  Osteodystrophy, unspecified

756.51  Osteogenesis imperfecta

Fragilitas ossium

Osteopsathyrosis

756.52  Osteopetrosis

756.53  Osteopoikilosis

756.54  Polyostotic fibrous dysplasia of bone

756.55  Chondroectodermal dysplasia

Ellis-van Creveld syndrome

756.56  Multiple epiphyseal dysplasia

756.59  Other

Albright (-McCune)-Sternberg syndrome

756.6    Anomalies of diaphragm

Absence of diaphragm

Congenital hernia:

diaphragmatic

foramen of Morgagni

Eventration of diaphragm

Excludes: congenital hiatus hernia (750.6)

756.7    Anomalies of abdominal wall

756.70  Anomaly of abdominal wall, unspecified

756.71  Prune belly syndrome

Eagle-Barrett syndrome

Prolapse of bladder mucosa

756.72  Omphalocele

Exomphalos

756.73  Gastroschisis

756.79  Other congenital anomalies of abdominal wall

Excludes: umbilical hernia (551-553 with.1)

756.8    Other specified anomalies of muscle, tendon, fascia, and connective tissue

756.81  Absence of muscle and tendon

Absence of muscle (pectoral)

756.82  Accessory muscle

756.83  Ehlers-Danlos syndrome

756.89  Other

Amyotrophia congenita

Congenital shortening of tendon

756.9    Other and unspecified anomalies of musculoskeletal system

Congenital:

anomaly NOS of musculoskeletal system, NEC

deformity NOS of musculoskeletal system, NEC

757       Congenital anomalies of the integument                 (ICD 9 CM Codes)

Includes:     anomalies of skin, subcutaneous tissue, hair, nails, and breast

Excludes:    hemangioma (228.00-228.09)

pigmented nevus (216.0-216.9)

757.0    Hereditary edema of legs

Congenital lymphedema

Hereditary trophedema

Milroy's disease

757.1    Ichthyosis congenita

Congenital ichthyosis

Harlequin fetus

Ichthyosiform erythroderma

757.2    Dermatoglyphic anomalies

Abnormal palmar creases

757.3    Other specified anomalies of skin

757.31  Congenital ectodermal dysplasia

757.32  Vascular hamartomas

Birthmarks

Port-wine stain

Strawberry nevus

757.33  Congenital pigmentary anomalies of skin

Congenital poikiloderma

Urticaria pigmentosa

Xeroderma pigmentosum

Excludes: albinism (270.2)

757.39  Other

Accessory skin tags, congenital

Congenital scar

Epidermolysis bullosa

Keratoderma (congenital)

Excludes: pilonidal cyst (685.0-685.1)

757.4    Specified anomalies of hair

Congenital:

alopecia

atrichosis

beaded hair

hypertrichosis

monilethrix

Persistent lanugo

757.5    Specified anomalies of nails

Anonychia

Congenital:

clubnail

koilonychia

leukonychia

onychauxis

pachyonychia

757.6    Specified congenital anomalies of breast

Accessory breast or nipple

Congenital absent breast or nipple

Supernumerary breast or nipple

Excludes: absence of pectoral muscle (756.81)

hypoplasia of breast (611.82)

micromastia (611.82)

757.8    Other specified anomalies of the integument

757.9    Unspecified anomaly of the integument

Congenital:

anomaly NOS of integument

deformity NOS of integument

758       Chromosomal anomalies                 (ICD 9 CM Codes)

Includes:     syndromes associated with anomalies in the number and form of chromosomes

Use additional codes for conditions associated with the chromosomal anomalies

758.0    Down's syndrome

Mongolism

Translocation Down's syndrome

Trisomy:

21 or 22

G

758.1    Patau's syndrome

Trisomy:

13

D1

758.2    Edward's syndrome

Trisomy:

18

E3

758.3    Autosomal deletion syndromes

758.31  Cri-du-chat syndrome

Deletion 5p

758.32  Velo-cardio-facial syndrome

Deletion 22q11.2

758.33  Other microdeletions

Miller-Dieker syndrome

Smith-Magenis syndrome

758.39  Other autosomal deletions

758.4    Balanced autosomal translocation in normal individual

758.5    Other conditions due to autosomal anomalies

Accessory autosomes NEC

758.6    Gonadal dysgenesis

Ovarian dysgenesis

Turner's syndrome

XO syndrome

Excludes: pure gonadal dysgenesis (752.7)

758.7    Klinefelter's syndrome

XXY syndrome

758.8    Other conditions due to chromosome anomalies

758.81  Other conditions due to sex chromosome anomalies

758.89  Other

758.9    Conditions due to anomaly of unspecified chromosome

759       Other and unspecified congenital anomalies         (ICD 9 CM Codes)

759.0    Anomalies of spleen

Aberrant spleen

Absent spleen

Accessory spleen

Congenital splenomegaly

Ectopic spleen

Lobulation of spleen

759.1    Anomalies of adrenal gland

Aberrant adrenal gland

Absent adrenal gland

Accessory adrenal gland

Excludes: adrenogenital disorders (255.2)

congenital disorders of steroid metabolism (255.2)

759.2    Anomalies of other endocrine glands

Absent parathyroid gland

Accessory thyroid gland

Persistent thyroglossal or thyrolingual duct

Thyroglossal (duct) cyst

Excludes: congenital:

goiter (246.1)

hypothyroidism (243)

759.3    Situs inversus

Situs inversus or transversus:

abdominalis

thoracis

Transposition of viscera:

abdominal

thoracic

Excludes: dextrocardia without mention of complete transposition (746.87)

759.4    Conjoined twins

Craniopagus

Dicephalus

Pygopagus

Thoracopagus

Xiphopagus

759.5    Tuberous sclerosis

Bourneville's disease

Epiloia

759.6    Other hamartoses, NEC

Syndrome:

Peutz-Jeghers

Sturge-Weber (-Dimitri)

von Hippel-Lindau

Excludes: neurofibromatosis (237.70-237.79)

759.7    Multiple congenital anomalies, so described

Congenital:

anomaly, multiple NOS

deformity, multiple NOS

759.8    Other specified anomalies

759.81  Prader-Willi syndrome

759.82  Marfan syndrome

759.83  Fragile X syndrome

759.89  Other

Congenital malformation syndromes affecting multiple systems, NEC

Laurence-Moon-Biedl syndrome

759.9    Congenital anomaly, unspecified

  (ICD 9 CM Codes)