759.89 SPECFIED CONG ANOMAL NEC

Synonyms

• Aarskog syndrome
• Aase syndrome
• Abnormal fetal duplication
• Abnormal fetus
• Acardia
• Acardiac monster
• Acardiacus anceps
• Acephalobrachius
• Acephalocheiria
• Acephalorhachia
• Acephalothorax
• Acquired and/or congenital pulmonary valve atresia
• Acquired mucociliary clearance defect
• Adams-Oliver syndrome
• Agnathus
• Allemann's syndrome
• Alport syndrome-like hereditary nephritis
• Alstrom syndrome
• Anadidymus
• Andersen Tawil syndrome
• Angelman syndrome
• Arteriohepatic dysplasia
• Asymmetric crying face association
• Atretocephalus
• Autositic monster
• Bannayan syndrome
• Bardet-Biedl syndrome
• Beckwith-Wiedemann syndrome
• Biemond's syndrome
• Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
• Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type
• Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type
• Borjeson-Forssman-Lehmann syndrome
• Brachydactyly syndrome type C
• Branchiooculofacial syndrome
• Cardio-acral-facial syndrome
• Cardio-facio-cutaneous syndrome
• Carpenter's syndrome
• Caudal dysplasia sequence
• Celosomial monster
• Cerebro-costo-mandibular syndrome
• Cerebrofacial dysplasia
• Cerebro-oculo-facio-skeletal syndrome
• Child syndrome
• Chimera
• Chronic infantile neurological, cutaneous and articular syndrome
• Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis
• Cleft palate lateral synechia syndrome
• Cockayne syndrome
• Coffin-Lowry syndrome
• Coffin-Siris syndrome
• Cohen syndrome
• Cole-Carpenter dysplasia
• Coloboma, heart malformation, choanal atresia, retardation of growth and development, genital abnormalities, and ear malformations association
• Congenital absence of heart structure
• Congenital anomaly of trunk
• Congenital cataracts, facial dysmorphism and neuropathy
• Congenital contractural arachnodactyly
• Congenital deafness with labyrinthine aplasia, microtia and microdontia
• Congenital iodine deficiency syndrome
• Congenital iodine deficiency syndrome - mixed type
• Congenital iodine deficiency syndrome - neurological type
• Congenital malformation syndromes with metabolic disturbances
• Congenital muscular hypertrophy-cerebral syndrome
• Congenital sequelae of disorders
• Congenital stenosis
• Congenital viral hepatitis
• Cranial duplication
• Craniofacial deafness hand syndrome
• Cranio-orbito-ocular dysraphia syndrome
• Cross syndrome
• Cryopyrin associated periodic syndrome
• Cryptodidymus
• Currarino triad
• Cutis gyrata syndrome of Beare and Stevenson
• Cyclopia
• Cyclops hypognathus
• Cylindrical embryo
• Danon disease
• De Lange syndrome
• Deafness-dystonia-optic neuronopathy syndrome
• Derencephalus
• Diaphragmatic hernia, abnormal face and distal limb anomalies
• Diaphragmatic hernia-exomphalos-hypertelorism syndrome
• Dipodia
• Double monster
• Duane-radial ray syndrome
• Duhamel's syndrome
• Dyggve-Melchior-Clausen syndrome
• Dysmorphic sialidosis, congenital form
• Ear, patella, short stature syndrome
• Ectopic fetus
• Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome
• Epstein syndrome
• Escobar syndrome
• Ethmocephalus
• Exstrophy of cloaca sequence
• Facial milia, lobate tongue, lingual and labial frenula syndrome
• Facio-auriculo-vertebral spectrum
• Femoral hypoplasia - unusual facies syndrome
• Fetal aminopterin syndrome
• Fetal hydantoin syndrome
• Fetal methyl mercury syndrome
• Fetal trimethadione syndrome
• Fetal valproate syndrome
• Fetal warfarin syndrome
• FG syndrome
• First arch syndrome
• Floating-Harbor syndrome
• Frasier syndrome
• Freeman-Sheldon syndrome
• Frontometaphyseal dysplasia
• Gardner syndrome
• Geleophysic dysplasia
• Genitopatellar syndrome
• Geroderma osteodysplastica
• Gillespie syndrome
• Gorlin-Chaudhry-Moss syndrome
• Grebe syndrome
• Grob's syndrome
• Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death
• Hand-foot-genital syndrome
• Hanhart's syndrome
• Hecht syndrome
• Hemihypertrophy of muscle
• Hereditary nephritis
• Holoacardius acephalus
• Holoacardius acormus
• Holoacardius amorphus
• Holt-Oram syndrome
• Homologous chimera
• Hyperhidrosis, premature cavities and premolar aplasia
• Hyperthermia-induced defect
• Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities
• Ileoumbilical fistula
• Immotile cilia syndrome due to defective radial spokes
• Immotile cilia syndrome due to excessively long cilia
• Immunodeficiency associated with multiple organ system abnormalities
• Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome
• Iris coloboma with ptosis, hypertelorism, and mental retardation
• Isologous chimera
• Johanson-Blizzard syndrome
• Kenny syndrome
• Klippel-Trenaunay-Weber syndrome
• Knuckle pads, deafness AND leukonychia syndrome
• Laminar heterotopia
• Langer-Giedion syndrome
• Larsen syndrome
• Laterality sequence
• Lenz microphthalmia syndrome
• Lethal Kniest-like syndrome
• Lethal multiple pterygium syndrome
• Levy-Hollister syndrome
• Limb reduction-ichthyosis syndrome
• Loeys-Dietz syndrome
• Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome
• Macrocephaly-capillary malformation
• Manitoba oculotrichoanal syndrome
• Marchesani syndrome
• Marden Walker syndrome
• Marfanoid joint hypermobility syndrome
• Marshall syndrome
• Marshall-Smith syndrome
• Maternal phenylketonuria fetal effect
• Meckel-Gruber syndrome
• Megalencephaly-capillary malformation syndrome
• Melnick-Fraser syndrome
• Menkes kinky-hair syndrome
• Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa
• Mermaid sirenomelia
• Microcephaly-capillary malformation syndrome
• Microcephaly-oculo-digito-esophageal-duodenal syndrome
• Midline facial cleft - Tessier cleft 30
• Mietens syndrome
• Miller syndrome
• Mohr syndrome
• Monocephalus tetrapus dibrachius
• Monster
• Monster with cranial anomalies
• Moore-Federman syndrome
• Mowat-Wilson syndrome
• Mulibrey nanism syndrome
• Multiple malformation syndrome due to non-infectious environmental agents
• Multiple malformation syndrome with early overgrowth
• Multiple malformation syndrome with facial defects as major feature
• Multiple malformation syndrome with facial-limb defects as major feature
• Multiple malformation syndrome with limb defect as major feature
• Multiple malformation syndrome with senile-like appearance
• Multiple malformation syndrome with unusual brain and/or neuromuscular findings
• Multiple malformation syndrome, moderate short stature, facial
• Multiple malformation syndrome, small stature, without skeletal dysplasia
• MVRCS association
• Myhre syndrome
• Nail-patella syndrome
• Nance-Horan syndrome
• Neu-Laxova syndrome
• Neurocutaneous syndrome
• Nodular embryo
• Noonan's syndrome
• Oculo-cerebro-cutaneous syndrome
• Oculodental syndrome
• Oculodentodigital syndrome
• Oculodento-osseous dysplasia
• Oculodento-osseous dysplasia - mild type
• Oculodento-osseous dysplasia - severe type
• Oculofaciocardiodental syndrome
• Oculo-palato-digital syndrome
• Oculoskeletal dysplasia
• Oral-facial-digital syndrome
• Oromandibular-limb hypogenesis spectrum
• Osteochondrodysplasia with osteopetrosis
• Otocephalic syndrome
• Oto-onycho-peroneal syndrome
• Oto-palato-digital syndrome, type I
• Oto-palato-digital syndrome, type II
• Otospondylomegaepiphyseal dysplasia
• Pallister-Hall syndrome
• Papillon-Lefèvre syndrome
• Parasitic monster
• Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits
• Pena-Shokeir phenotype
• Pentalogy of Cantrell
• Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome
• Pili torti-deafness syndrome
• Podencephalus
• Polysomatous monster
• Port-wine stain in Rubinstein-Taybi syndrome
• Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome
• Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
• Progeroid short stature with pigmented nevi
• Progressive hereditary glomerulonephritis without deafness
• Proteus syndrome
• Radial aplasia-thrombocytopenia syndrome
• Radiation chimera
• RAPADILINO syndrome
• Renal coloboma syndrome
• Renal dysplasia and retinal aplasia
• Renpenning syndrome
• Retinal detachment and occipital encephalocele
• Retinoic acid embryopathy
• Robinow syndrome
• Robinson nail dystrophy-deafness syndrome
• Rothmund-Thomson syndrome
• Royer's syndrome
• Rubinstein-Taybi syndrome
• Rud's syndrome
• Russell-Silver syndrome
• Rutland ciliary disorientation syndrome
• Ruvalcaba syndrome
• Ruvalcaba-Myhre syndrome
• Saldino-Mainzer dysplasia
• Schinzel-Giedion syndrome
• Schwartz syndrome
• Schwartz-Jampel syndrome
• Seckel syndrome
• Secondary ciliary dyskinesia
• Senter syndrome
• Shprintzen syndrome
• Simpson-Golabi-Behmel syndrome
• Single monster
• Sirenoform monster
• Sirenomelia sequence
• Smith-Lemli-Opitz syndrome
• Spondyloenchondrodysplasia with immune dysregulation
• Stickler syndrome
• Stunted embryo
• Suspect cystic fibrosis fetus
• Symphalangism-brachydactyly syndrome
• Synotus
• Thalidomide embryopathy syndrome
• Thoracoceloschisis
• Timothy syndrome type 1
• Townes syndrome
• Transient mucociliary clearance defect
• Tricho-dento-osseous syndrome
• Trichohepatoenteric syndrome
• Trichorhinophalangeal dysplasia type I
• Trichorhinophalangeal syndrome
• Tricho-thiodystrophy
• Triplet monster
• Type III short rib polydactyly syndrome
• Ulnar mammary syndrome
• Umbilical fistula
• Venous-lymphatic malformation
• Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome
• Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association
• Warburg syndrome
• Warsaw breakage syndrome
• Weaver syndrome
• Weill-Marchesani syndrome
• Wildervanck's syndrome
• Williams syndrome
• Wissler-Fanconi syndrome
• X-linked mental retardation syndrome, Christianson type
• Young's syndrome
• Zimmermann-Laband syndrome

References to Index of Diseases and Injuries

The code 759.89 has the following ICD-9-CM references to the Index of Diseases and Injuries

• 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 747.31
    • 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 747.31
    • 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 752.43
    • 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) 747.31
    • 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 752.31
    • acquired 621.8
  • vagina (acquired) 623.2
    • congenital (total) (partial) 752.45
    • 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 intellectual disabilities) 759.89

• Birt-Hogg-Dube syndrome 759.89

• Brachman-de Lange syndrome (Amsterdam dwarf, intellectual disabilities, and brachycephaly) 759.89

• Brachymorphism and ectopia lentis 759.89

• Bruck-de Lange disease or syndrome (Amsterdam dwarf, intellectual disabilities, 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, intellectual disabilities, 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, intellectual disabilities, and brachycephaly) 759.89

• Disease, diseased - see also Syndrome
  • Bruck-de Lange (Amsterdam dwarf, intellectual disabilities, and brachycephaly) 759.89
  • Cockayne's (microcephaly and dwarfism) 759.89
  • Kok 759.89
  • lymphoproliferative (chronic) (M9970/1) 238.79
    • X linked 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

• Glaucoma (capsular) (inflammatory) (noninflammatory) (primary) 365.9
  • in or with
    • congenital syndromes NEC 759.89 [365.44]

• 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
  • angiolymphoid, with eosinophilia (ALHE) 228.01
  • 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 747.31
    • 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) 752.43
  • 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 747.32
    • artery 747.31
    • 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 752.32
  • vagina 752.45
  • 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 intellectual disabilities) 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-L�age 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 (see also Complications, transfusion) 999.70
  • 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 intellectual disabilities) 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 intellectual disabilities) 759.89
  • Barth 759.89
  • basal cell nevus 759.89
  • Beckwith (-Wiedemann) 759.89
  • Biedl-Bardet (obesity, polydactyly, and intellectual disabilities) 759.89
  • Biemond's (obesity, polydactyly, and intellectual disabilities) 759.89
  • Birt-Hogg-Dube 759.89
  • Borjeson-Forssman-Lehmann 759.89
  • Brachman-de Lange (Amsterdam dwarf, intellectual disabilities, and brachycephaly) 759.89
  • cardiofaciocutaneous 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, intellectual disabilities, and brachycephaly) (Cornelia) 759.89
  • Fraser's 759.89
  • Freeman-Sheldon 759.89
  • Gillespie's (dysplasia oculodentodigitalis) 759.89
  • Gorlin-Chaudhry-Moss 759.89
  • Gorlin's 759.89
  • inverted Marfan's 759.89
  • Joubert 759.89
  • Kabuki 759.89
  • Klippel-Trenaunay 759.89
  • Laurence-Moon (-Bardet)-Biedl (obesity, polydactyly, and intellectual disabilities) 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-L�age and Psaume (orodigitofacial dysostosis) 759.89
  • pseudo-Turner's 759.89
  • Rubinstein-Taybi's (brachydactylia, short stature, and intellectual disabilities) 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

Crosswalk Information

The code 759.89 converts into the following ICD-10 code(s):

ICD-9 Code		ICD-10 Code	ICD-10 Description
759.89		E78.71	Barth syndrome
		E78.72	Smith-Lemli-Opitz syndrome
		Q87.2	Congenital malformation syndromes predom involving limbs
		Q87.3	Congenital malformation syndromes involving early overgrowth
		Q87.5	Oth congenital malformation syndromes w oth skeletal changes
		Q87.81	Alport syndrome
		Q87.89	Oth congenital malformation syndromes, NEC
		Q89.8	Other specified congenital malformations

Similar Codes