List of ICD-9 codes 740-759: congenital anomalies Information & List of ICD-9 codes 740-759: congenital anomalies Links at HealthHaven.com

List of ICD-9 codes 740-759: congenital anomalies Information & List of ICD-9 codes 740-759: congenital anomalies Links at HealthHaven.com

advertise
add site
services
publishers
database
health videos

search wiki for ?

web dir firms image gallery news pdf wiki shop video

about
toolbar
stats
live show
health store
more stuff
JOIN/LOGIN

Featured Results:

Conditions and Diseases: Congenital Anomalies , directory for Conditions...

Conditions and Diseases: Congenital Anomalies, directory for Conditions...
healthysense.com

Congenital anomalies alphabetical list ing

Congenital anomalies alphabetical listing
eatonhand.com

Flash Code ICD CPT Coding Software

Flash Code ICD CPT Coding Software
physicianswebsites.com

Congenital Anomalies - Advances in Management, August 1, 2009

Congenital Anomalies - Advances in Management, August 1, 2009
ccspublishing.com

Contents

1 14. Congenital anomalies (740-759)
2 See also

[edit] 14. Congenital anomalies (740-759)

[edit] nervous system

(740) Anencephalus and similar anomalies
- (740.0) Anencephalus

(741) Spina bifida

(742) Other congenital anomalies of nervous system
- (742.1) Microcephalus
- (742.3) Hydrocephalus

[edit] eye, ear, face and neck

(743) Congenital anomalies of eye
- (743.0) Anophthalmos
- (743.1) Microphthalmos
- (743.2) Buphthalmos
- (743.3) Congenital cataract and lens anomalies
- (743.4) Coloboma and other anomalies of anterior segment
  - (743.45) Aniridia
- (743.5) Congenital anomalies of posterior segment
- (743.6) Congenital anomalies of eyelids, lacrimal system, and orbit

(744) Congenital anomalies of ear, face, and neck
- (744.0) Anomalies of ear causing impairment of hearing
- (744.1) Accessory auricle
- (744.2) Other specified congenital anomalies of ear
  - (744.22) Macrotia
  - (744.23) Microtia
- (744.3) Unspecified congenital anomaly of ear
- (744.4) Branchial cleft cyst or fistula; preauricular sinus
- (744.5) Webbing of neck
- (744.8) Other specified congenital anomalies of face and neck
  - (744.81) Macrocheilia
  - (744.82) Microcheilia
  - (744.83) Macrostomia
  - (744.84) Microstomia

[edit] circulatory system

(745) Bulbus cordis anomalies and anomalies of cardiac septal closure
- (745.4) Ventricular septal defect
- (745.5) Atrial septal defect

(746) Other congenital anomalies of heart

(747) Other congenital anomalies of circulatory system
- (747.1) Coarctation of aorta
  - (747.11) Interruption of aortic arch
- (747.2) Other congenital anomalies of aorta
- (747.3) Congenital anomalies of pulmonary artery
- (747.4) Congenital anomalies of great veins
- (747.5) Absence or hypoplasia of umbilical artery
- (747.6) Arteriovenous malformation, unspec.
- (747.8) Other specified anomalies of circulatory system
  - (747.81) Arteriovenous malformation of brain
  - (746.82) Cor triatriatum
  - (746.83) Infundibular pulmonic stenosis congenital
  - (746.84) Congenital obstructive anomalies of heart not elsewhere classified
  - (746.85) Coronary artery anomaly congenital
  - (746.86) Congenital heart block
  - (746.87) Malposition of heart and cardiac apex
  - (747.89) Other specified congenital anomalies of heart
    - Brugada syndrome
- (747.9) Unspecified congenital anomaly of circulatory system

[edit] respiratory system

(748) Congenital anomalies of respiratory system
- (748.0) Choanal atresia

[edit] digestive system

(749) Cleft palate
- (749.0) Cleft palate, unspec.
- (749.2) Cleft palate w/ cleft lip

(750) Other congenital anomalies of upper alimentary tract
- (750.0) Tongue tie
- (750.5) Pyloric stenosis

(751) Other congenital anomalies of digestive system

[edit] genital organs

(752) Congenital anomalies of genital organs
- (752.4) Anomalies of cervix, vagina, and external female genitalia
  - (752.42) Imperforate hymen
- (752.5) Undescended testicle
- (752.6) Hypospadias and epispadias
  - (752.61 Hypospadias
  - (752.62 Epispadias
  - (752.63 Congenital chordee
  - (752.64 Micropenis

[edit] urinary system

(753) Congenital anomalies of urinary system
- (753.0) Renal agenesis and dysgenesis
- (753.1) Cystic kidney disease
- (753.2) Obstructive defects of renal pelvis and ureter
- (753.3) Other specified anomalies of kidney
  - Renal ectopia
  - Horseshoe kidney
- (753.4) Other specified anomalies of ureter
  - Ectopic ureter
- (753.5) Exstrophy of urinary bladder
- (753.6) Atresia and stenosis of urethra and bladder neck
- (753.7) Anomalies of urachus
  - Urachal cyst
- (753.8) Other specified anomalies of bladder and urethra
- (753.9) Unspecified anomaly of urinary system

[edit] musculoskeletal system

(754) Certain congenital musculoskeletal deformities
- (754.1) Torticollis, sternomastoid
- (754.3) Dislocation of hip, unilateral
- (754.5) Varus deformities of feet
  - (754.51) Talipes equinovarus
- (754.6) Valgus deformities of feet
- (754.8) Other specified nonteratogenic anomalies
  - (754.81) Pectus excavatum

(755) Other congenital anomalies of limbs
- (755.0) Polydactyly
- (755.5) Other congenital anomalies of upper limb including shoulder girdle
  - (755.55) Acrocephalosyndactyly
    - Apert syndrome
- (755.9) Limb anomaly, unspec.

(756) Other congenital musculoskeletal anomalies
- (756.1) Anomalies of spine
  - (756.12) Spondylolisthesis
  - (756.17) Spina bifida occulta
- (756.5) Osteodystrophies
  - (756.51) Osteogenesis imperfecta
- (756.6) Congenital anomalies of diaphragm
- (756.7) Congenital anomalies of abdominal wall

[edit] integument

(757) Congenital anomalies of the integument
- (757.3) Other specified anomalies of skin
  - (757.32) Birthmarks
  - (757.39) Other specified congenital anomalies of skin
- (757.6) Supernumerary nipple

[edit] chromosomal anomalies

(758) Chromosomal anomalies
- (758.0) Down syndrome
- (758.1) Patau's syndrome
- (758.2) Edward's syndrome
- (758.3) Autosomal deletion syndromes
  - (758.31) Cri du chat
  - (758.32) Velo-cardio-facial syndrome
  - (758.33) Other microdeletions
    - Miller-Dieker syndrome
    - Smith-Magenis syndrome
- (758.4) Balanced autosomal translocation in normal individual
- (758.5) Other conditions due to autosomal anomalies
- (758.6) Gonadal dysgenesis
  - Turner's syndrome
  - XO syndrome
- (758.7) Klinefelter's syndrome
- (758.8) Other conditions due to sex chromosome anomalies
- (758.9) Conditions due to anomaly of unspecified chromosome

[edit] Other

(759) Other and unspecified congenital anomalies
- (759.0) Anomalies of spleen, congenital
- (759.1) Anomalies of adrenal gland, congenital
- (759.2) Anomalies of other endocrine glands, congenital
- (759.3) Situs inversus
- (759.4) Conjoined twins
- (759.5) Tuberous sclerosis
- (759.6) Other congenital hamartoses, not elsewhere classified
  - Cowden syndrome
- (759.7) Multiple congenital anomalies, so described
- (759.8) Other specified congenital anomalies
  - (759.81) Prader-Willi syndrome
  - (759.82) Marfan syndrome
  - (759.83) Fragile X syndrome
  - (759.89) Other specified congenital anomalies
- (759.9) Congenital anomaly, unspecified

[edit] See also

Pathology: Medical conditions (Diseases/Disorders/Illness, Syndromes/Sequences, Symptoms/Signs, Injuries, etc.) and ICD codes

Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease (Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis

(C/D,
140-239 & 280-289)

Cancer (C00-D48, 140-239)	Tumor

Myeloid hematologic (D50-D77, 280-289)	Anemia · Coagulopathy

Lymphoid immune (D80-D89, 279)	Immunodeficiency · Immunoproliferative disorder · Hypersensitivity

Endocrine disease · Nutrition disorder · Inborn error of metabolism

Mental disorder

Nervous system disease (CNS, PNS) · Neuromuscular disease

Eye disease · Ear disease

Cardiovascular disease (Heart disease, Vascular disease)

Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)

Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach, Enteropathy, Liver, Pancreatic)

Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)

Musculoskeletal disorders · Osteochondropathy (Osteopathy, Chondropathy)

Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast disease · Female genital disease

Complications of pregnancy · Obstetric labor complication · Puerperal disorder

Congenital disorder

Syndromes · Medical signs (Eponymous)

Bone fracture · Joint dislocation · Sprain · Strain · subluxation · Head injury · Chest trauma · Poisoning

Congenital malformations and deformations of nervous system (Q00-Q07, 740-742)

Neural tube defect	Anencephaly (Acephaly, Acrania, Iniencephaly) · Encephalocele · Arnold-Chiari malformation

Other	Microcephaly · Congenital hydrocephalus (Dandy-Walker syndrome) other reduction deformities (Holoprosencephaly, Lissencephaly, Pachygyria, Hydranencephaly) Septo-optic dysplasia · Megalencephaly CNS cyst (Porencephaly, Schizencephaly) Polymicrogyria (Bilateral frontoparietal polymicrogyria)

Neural tube defect	Spina bifida · Rachischisis

Other	Currarino syndrome · Diastomatomyelia · Syringomyelia

central nervous system navs: anat/physio/dev, noncongen/congen/neoplasia, symptoms+signs/eponymous, proc

Congenital malformations and deformations of eyes (Q10-Q15, 743)

Eyelid	Ptosis · Ectropion · Entropion · Distichia · Blepharophimosis · Ablepharon · Marcus Gunn phenomenon

Lacrimal apparatus	Congenital lacrimal duct obstruction

Entire eye	Anophthalmia · Microphthalmia

Lens	Ectopia lentis · Aphakia

Iris	Aniridia

Anterior segment	Axenfeld syndrome

Cornea	Keratoglobus · Megalocornea

Other	Buphthalmos · Coloboma · Hydrophthalmos · Norrie disease

eye navs: anat/adnexa anat/pathways/physio/dev, noncongen/congen/neoplasia, eponymous signs, proc

v • d • e Congenital malformations and deformations of ears (Q16-Q17, 744.0-744.3)

Ears	Macrotia · Microtia · Low-set ears

ear navs: anat/pathways/physio/dev, noncongen/congen, eponymous signs, proc

v • d • e Congenital malformations and deformations of face and neck (Q18, 744.4-744.9)

Face	jaw: Otocephaly mouth: Macrostomia · Microstomia lip: Macrocheilia · Microcheilia multiple: Hallermann-Streiff syndrome

Neck	Webbed neck

mouth navs: anat/dev, noncongen/congen face/congen GI/neoplasia, symptoms, proc

Congenital heart defects (Q20-Q24, 745-746)

Cardiac shunt/
heart septal defect

Aortopulmonary septal defect	R→L: Double outlet right ventricle (Taussig-Bing syndrome) · Transposition of the great vessels (dextro, levo) · Persistent truncus arteriosus Aortopulmonary window

Atrial septal defect	L→R: Sinus venosus atrial septal defect · Lutembacher's syndrome

Ventricular septal defect	L→R and R→L: Eisenmenger's syndrome R→L, with other conditions: Tetralogy of Fallot

Atrioventricular septal defect	L→R: Ostium primum

Valvular heart disease/
heart chambers

Right	pulmonary valves (stenosis, insufficiency) · tricuspid valves (stenosis, atresia, Ebstein's anomaly) · Hypoplastic right heart syndrome

Left	aortic valves (stenosis, insufficiency, bicuspid) · mitral valves (stenosis, regurgitation) · Hypoplastic left heart syndrome

Other

Dextrocardia · Levocardia · Cor triatriatum · Crisscross heart · Brugada syndrome · Coronary artery anomaly · Ventricular inversion

heart navs: anat/physio/dev, noncongen/congen/neoplasia, symptoms+signs/eponymous, proc

Congenital malformations and deformations of respiratory system (Q30-Q34, 748)

Nose	Choanal atresia

Larynx	Laryngocele - Laryngomalacia

Trachea and bronchus	Tracheomalacia - Tracheal stenosis - Bronchomalacia - Mounier-Kuhn syndrome

Lung	Bronchiectasis - Pulmonary hypoplasia - Pulmonary sequestration - Congenital cystic adenomatoid malformation

respiratory system navs: anat nose,larynx/lower+thoracic cavity/physio/dev, noncongen/congen/tumors, symptoms+signs/eponymous, proc

Congenital malformations and deformations of digestive system (Q35-Q45, 749-751)

Tongue, mouth and pharynx	Cleft lip and palate · Van der Woude syndrome · tongue (Ankyloglossia, Macroglossia, Hypoglossia)

Esophagus	EA/TEF (Esophageal atresia: types A, B, C, and D, Tracheoesophageal fistula: types B, C, D and E) esophageal rings (Esophageal web · upper, Schatzki ring · lower)

Stomach	Pyloric stenosis · Hiatus hernia

Intestines	Intestinal atresia (Duodenal atresia) · Meckel's diverticulum · Hirschsprung's disease · Intestinal malrotation · Dolichocolon · Enteric duplication cyst

Rectum/anus	Imperforate anus · Persistent cloaca

Pancreas	Annular pancreas · Accessory pancreas · Johanson-Blizzard syndrome Pancreas divisum

Bile duct	Choledochal cysts (Caroli disease) · Biliary atresia

Liver	Alagille syndrome

mouth navs: anat/dev, noncongen/congen face/congen GI/neoplasia, symptoms, proc
digestive system navs: anat of tract,glands,perit,diaphragm/physio/dev, noncongen/congen/congen of d+w/neoplasia, symptoms+signs/eponymous, proc

Congenital malformations and deformations of sex organs (Q50-Q56 · 752)

Uterine malformation	Müllerian agenesis · Unicornuate uterus · Uterus didelphys · Bicornuate uterus · Uterine septum · Arcuate uterus

Other	Vaginal septum · Clitoromegaly

Testicle	Cryptorchidism · Polyorchidism · Monorchism · Anorchia · Sertoli cell-only syndrome

Penis	Hypospadias · Chordee · Micropenis · Macropenis · Penile agenesis · Diphallia

Vas deferens	Congenital absence of the vas deferens

Pseudohermaphroditism · True hermaphroditism · Mixed gonadal dysgenesis · Swyer syndrome · Persistent Mullerian duct syndrome

reproductive system navs: anat female,male/physio/dev, noncongen/congen/neoplasia, symptoms+signs/eponymous, proc

Congenital malformations and deformations of urinary system (Q60-Q64, 753)

Abdominal

Kidney	Renal agenesis/Potter sequence, Papillorenal syndrome cystic (Polycystic kidney disease, Meckel syndrome, Multicystic dysplastic kidney, Medullary sponge kidney) Horseshoe kidney - Renal ectopia - Nephronophthisis Dent's disease - Alport syndrome

Ureter	Ectopic ureter - Megaureter

Pelvic

Bladder	Bladder exstrophy

Urethra	Epispadias - Hypospadias

Vestigial

urinary system navs: anat/physio/dev, noncongen/acid+base/congen/neoplasia, symptoms+signs/eponymous, proc

Congenital malformations and deformations of musculoskeletal system / musculoskeletal abnormality (Q65-Q76, 754-756.3)

Upper	clavicle/shoulder: Cleidocranial dysostosis · Sprengel's deformity · Wallis Zieff Goldblatt syndrome hand deformity: Madelung's deformity · Clinodactyly

Lower	hip: Dislocation of hip/Hip dysplasia · Upington disease · Coxa valga · Coxa vara knee: Genu valgum · Genu varum foot deformity: Club foot · Flat feet · Pes cavus · Rocker bottom foot

Either/both	dactyly/digit: Polydactyly/Syndactyly (Webbed toes) · Arachnodactyly · Cenani Lenz syndactylism · Ectrodactyly · Brachydactyly reduction deficits/limb: Acheiropodia · ectromelia (Phocomelia, Amelia, Hemimelia) multiple joints: Arthrogryposis · Larsen syndrome · Rapadilino syndrome

Craniosynostosis: Scaphocephaly · Oxycephaly · Trigonocephaly

Craniofacial dysostosis: Crouzon syndrome · Hypertelorism · Hallermann-Streiff syndrome · Treacher Collins syndrome

other: Macrocephaly · Platybasia · Craniodiaphyseal dysplasia · Dolichocephaly · Greig cephalopolysyndactyly syndrome · Plagiocephaly · Saddle nose

Other axial

spine: spinal curvature (Scoliosis) · Klippel-Feil syndrome · Spondylolisthesis · Spina bifida occulta

ribs: Cervical rib · Bifid rib

sternum: Pectus excavatum · Pectus carinatum

joint navs: anat, non-congenital arthropathies/deformities/dorsopathies/soft tissue arthropathy/congenital, eponymous signs, proc

Osteochondrodysplasia (Q77-Q78, 756.4-756.5)

Osteodysplasia/
osteodystrophy

Diaphysis	Camurati-Engelmann disease/Engelmann syndrome

Metaphysis	Metaphyseal dysplasia · Jansen's metaphyseal chondrodysplasia · Schmid metaphyseal chondrodysplasia

Epiphysis	Spondyloepiphyseal dysplasia congenita · Multiple epiphyseal dysplasia · Otospondylomegaepiphyseal dysplasia

Osteosclerosis	Raine syndrome · Osteopoikilosis · Osteopetrosis

Other/ungrouped	FLNB (Boomerang dysplasia) · Polyostotic fibrous dysplasia (McCune-Albright syndrome)

Chondrodysplasia/
chondrodystrophy
(including dwarfism)

bone and cartilage navs: anat/physio/dev, noncongen/congen/neoplasia, symptoms+signs/eponymous signs, proc

v • d • e Congenital diaphragm and abdominal wall defects, abdominopelvic cavity (Q79.0-Q79.5, 756.6-756.7)

Thoracic diaphragm	Hernia: Congenital diaphragmatic hernia (Bochdalek hernia)

Abdominal wall	Omphalocele · Gastroschisis · Prune belly syndrome

digestive system navs: anat of tract,glands,perit,diaphragm/physio/dev, noncongen/congen/congen of d+w/neoplasia, symptoms+signs/eponymous, proc

Congenital malformations and deformations of integument (Q80-Q82, 757.0-757.3)

Skin disease/
genodermatosis

Congenital ichthyosis

AD	Ichthyosis vulgaris

AR	Congenital ichthyosiform erythroderma: Epidermolytic hyperkeratosis · Ichthyosis lamellaris (Harlequin type ichthyosis) Netherton syndrome · Zunich-Kaye syndrome · Sjögren-Larsson syndrome

XR	X-linked ichthyosis

Epidermolysis bullosa

Epidermolysis bullosa simplex · Junctional epidermolysis bullosa · Epidermolysis bullosa dystrophica

Pigmentation disorder

Incontinentia pigmenti · Urticaria pigmentosa · Lelis syndrome

DNA repair-deficiency disorder

Bloom syndrome · Rothmund-Thomson syndrome · Xeroderma pigmentosum

Ectodermal dysplasia

Naegeli syndrome/Dermatopathia pigmentosa reticularis · Hay-Wells syndrome · Hypohidrotic ectodermal dysplasia · Focal dermal hypoplasia · Ellis-van Creveld syndrome

Hyperkeratosis/keratinopathy

Meleda disease · Keratosis pilaris · Darier's disease · Dyskeratosis congenita · Lelis syndrome

Capillary hemangioma · Port-wine stain (Nevus flammeus nuchae)

Other

Familial cutaneous papillomatosis · Kindler syndrome · cadherin (EEM syndrome) · immune system (Hereditary lymphedema, Mastocytosis) · Hailey Hailey · Birthmark

Elastic fiber/Connective tissue

Cutis laxa (Gerodermia osteodysplastica) · Pseudoxanthoma elasticum

integument, SF, LCT navs: anat/physio, noncongen/congen/neoplasia, symptoms+signs/eponymous, proc

v • d • e Congenital malformations and deformations of skin appendages (Q84, 757.4-757.5)

Nail disease	Anonychia · Leukonychia · Pachyonychia congenita/Onychauxis · Koilonychia

Hair disease	keratin disease (Monilethrix) · Sabinas brittle hair syndrome · Pili annulati · Uncombable hair syndrome

skin appendage navs: anat, noncongen/congen/neoplasia, symptoms+signs/eponymous, proc

v • d • e Congenital malformations and deformations of the breast (Q83, 757.6)

Breast	Amastia · Polymastia · Micromastia

Nipple	Athelia · Polythelia

breast navs: anat/physio, noncongen/congenital/neoplasia, proc

Pathology: chromosome abnormalities (Q90-Q99 · 758)

Trisomies	Down syndrome (21) · Edwards syndrome (18) · Patau syndrome (13) Trisomy 9 · Warkany syndrome 2 (8) · Trisomy 22/Cat eye syndrome (22) · Trisomy 16

Monosomies/deletions	Wolf-Hirschhorn syndrome (4) · Cri du chat/Chromosome 5q deletion syndrome (5) · Williams syndrome (7) · Jacobsen syndrome (11) · Miller-Dieker syndrome/Smith-Magenis syndrome (17) · Di George's syndrome (22) genomic imprinting (Angelman syndrome/Prader-Willi syndrome (15))

X/Y linked

Monosomy	Turner syndrome (XO)

Trisomy/tetrasomy, other karyotypes/mosaics	Klinefelter's syndrome (47,XXY) · 48,XXYY · 49,XXXXY Triple X syndrome (47,XXX) · 48,XXXX · 49,XXXXX 47,XYY

Leukemia/lymphoma

Lymphoid	Burkitt's lymphoma t(8 MYC;14 IGH) · Follicular lymphoma t(14 IGH;18 BCL2) · Mantle cell lymphoma/Multiple myeloma t(11 CCND1:14 IGH) · Anaplastic large cell lymphoma t(2 ALK;5 NPM1) · Acute lymphoblastic leukemia

Myeloid	Philadelphia chromosome t(9 ABL; 22 BCR) · Acute myeloblastic leukemia with maturation t(8 RUNX1T1;21 RUNX1) · Acute promyelocytic leukemia t(15 PML,17 RARA) · Acute megakaryoblastic leukemia t(1 RBM15;22 MKL1)

Other

Ewing's sarcoma t(11 FLI1; 22 EWS) · Synovial sarcoma t(x SYT;18 SSX) · Dermatofibrosarcoma protuberans t(17 COL1A1;22 PDGFB) · Myxoid liposarcoma t(12 DDIT3; 16 FUS) · Desmoplastic small round cell tumor t(11 WT1; 22 EWS) · Alveolar rhabdomyosarcoma t(2 PAX3; 13 FOXO1) t (1 PAX7; 13 FOXO1)

Gonadal dysgenesis

Mixed gonadal dysgenesis · XX gonadal dysgenesis

Other

Fragile X syndrome · Uniparental disomy

v • d • e Lymphatic disease: splenic disease (D73/Q89.0, 289.4-289.5/759.0)

Acquired	Acquired asplenia/hyposplenism · Wandering spleen · Splenomegaly (Banti's syndrome)

Congenital	Congenital asplenia/hyposplenism · Accessory spleen · Polysplenia

lymphatic organ navs: anat, physio, lymphatic disease/splenic disease/thymus disorders/thymus neoplasia/vascular tumors, proc

Congenital endocrine disease (Q89.1-Q89.2, 759.1-759.2)

see congenital digestive

Hypothalamic/
pituitary axes
+parathyroid

Pituitary	Congenital hypopituitarism

Thyroid	Persistent thyroglossal duct · Thyroglossal cyst Congenital hypothyroidism: Thyroid dysgenesis · Thyroid dyshormonogenesis (Pendred syndrome)

Parathyroid	Congenital absence of parathyroid

Adrenal	Absent adrenal gland

Gonads	see congenital reproductive

endocrine navs: anat/physio/dev/hormones, noncongen/congen/neoplasia, symptoms+signs/eponymous, proc

v • d • e Twin conditions (Q89.3-Q89.4, 759.3-759.4)

Zygosity	Monozygotic · Dizygotic · Half twin

Monochorionic twins	Twin-to-twin transfusion syndrome · Twin reversed arterial perfusion · Monoamniotic twins

Conjoined twins	Parasitic twin (Craniopagus parasiticus, Fetus in fetu)

Other	Vanishing twin · Chimerism

v • d • e Phakomatoses (Q85, 759.5-759.6)

Neurofibromatosis	Type I · Type II

Angiomatosis	Sturge-Weber syndrome · Von Hippel-Lindau disease

Hamartoma	Tuberous sclerosis · Hypothalamic hamartoma (Pallister-Hall syndrome) · Multiple hamartoma syndrome (Proteus syndrome, Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Lhermitte-Duclos disease)

Other	Abdallat Davis Farrage syndrome · Ataxia telangiectasia · Incontinentia pigmenti · Peutz-Jeghers syndrome

v • d • e Congenital abnormality · multiple abnormalities (Q87, 759.7)

Craniofacial	Acrocephalosyndactylia (Apert syndrome/Pfeiffer syndrome, Saethre-Chotzen syndrome, Carpenter syndrome, Sakati-Nyhan-Tisdale syndrome) other: Möbius syndrome · Goldenhar syndrome · Cyclopia

Short stature	Aarskog-Scott syndrome · Cockayne syndrome · Cornelia de Lange Syndrome · Dubowitz syndrome · Noonan syndrome · Robinow syndrome · Silver-Russell dwarfism · Seckel syndrome · Smith-Lemli-Opitz syndrome-Turner syndrome

Limbs	Adducted thumb syndrome · Holt-Oram syndrome · Klippel-Trénaunay-Weber syndrome · Nail-patella syndrome · Rubinstein-Taybi syndrome Gastrulation/mesoderm: Caudal regression syndrome · ectromelia (Sirenomelia) · VACTERL association

Overgrowth	Beckwith-Wiedemann syndrome · Sotos syndrome · Weaver syndrome

Laurence-Moon-Bardet-Biedl	Bardet-Biedl syndrome · Laurence-Moon syndrome

Combined/other, known locus	3 (Zimmerman-Laband syndrome) · 4/13 (Fraser syndrome) · 8 (Branchio-oto-renal syndrome) · 12 (Keutel syndrome, Timothy syndrome) · 15 (Marfan syndrome) · 19 (Donohue syndrome)

Combined/other, unknown locus	Ablepharon macrostomia syndrome · Fountain syndrome · Urban-Rogers-Meyer syndrome · Yunis-Varon syndrome

Retrieved from "http://en.wikipedia.org/wiki/List_of_ICD-9_codes_740-759:_congenital_anomalies"

Categories: Musculoskeletal disorders | Congenital disorders | Skeletal disorders | Hematology | Medical manuals

Product Results (view all...)

search wiki for ?

web dir firms image gallery news pdf wiki shop video

↑ top of page ↑

about thumbshots

free web stats

drupal statistics module