2011 ICD-9-CM Diagnosis Code 759.89

Other specified congenital anomalies

• A syndrome of mental retardation, retinitis pigmentosa, hypogonadism, and spastic paraplegia. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no longer considered as valid terms in that patients with Laurence and Moon had spastic paraplegia but no polydactyly and obesity which were the key elements in the Bardet and Biedl patients. Bardet-Biedl syndrome is a separate entity.
• Short description: Specfied cong anomal NEC.
• ICD-9-CM 759.89 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
• You are viewing the 2011 version of ICD-9-CM 759.89.
• More recent version(s) of ICD-9-CM 759.89: 2012 2013.

759.89 Alternative Terminology

• 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
• Anomalies of umbilicus
• 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
• Borjeson-forssman-lehmann syndrome
• Brachydactyly syndrome type c
• 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
• 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 contractural arachnodactyly
• 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 viral hepatitis
• Cranial duplication
• Cranio-orbito-ocular dysraphia syndrome
• Cross syndrome
• Cryopyrin associated periodic syndrome
• Cryptodidymus
• Currarino triad
• Cyclopia
• Cyclops hypognathus
• Cylindrical embryo
• Danon disease
• De lange syndrome
• Derencephalus
• Dipodia
• Double monster
• Duhamel's syndrome
• Dyggve-melchior-clausen syndrome
• Dysmorphic sialidosis, congenital form
• Ectopic fetus
• 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
• Geroderma osteodysplastica
• Gillespie syndrome
• Gorlin-chaudhry-moss syndrome
• Grebe syndrome
• Grob's syndrome
• Hanhart's syndrome
• Hecht syndrome
• Hemihypertrophy of muscle
• Hereditary nephritis
• Holoacardius
• 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
• 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
• Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome
• Marchesani syndrome
• Marfanoid joint hypermobility syndrome
• Marshall syndrome
• Marshall-smith syndrome
• Maternal pku fetal effect
• Meckel-gruber syndrome
• Melnick-fraser syndrome
• Menkes kinky-hair syndrome
• Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa
• Mermaid sirenomelia
• Midline facial cleft - tessier cleft 30
• Mietens syndrome
• Miller syndrome
• Mohr syndrome
• Monocephalus tetrapus dibrachius
• Monster
• Monster with cranial anomalies
• Moore-federman 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
• Nail-patella syndrome
• Nance-horan syndrome
• Neu-laxova syndrome
• Neurocutaneous syndrome
• Nodular embryo
• Noonan's syndrome
• Oculo-cerebro-cutaneous syndrome
• Oculodentodigital syndrome
• Oculodento-osseous dysplasia
• Oculodento-osseous dysplasia - mild type
• Oculodento-osseous dysplasia - severe type
• Oculo-palato-digital syndrome
• 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-lef�vre syndrome
• Parasitic monster
• Pena-shokeir phenotype
• Pentalogy of cantrell
• Pibids syndrome, photosensitivity with ibids
• Pili torti-deafness syndrome
• Podencephalus
• Polysomatous monster
• Port-wine stain in rubinstein-taybi syndrome
• Progeroid short stature with pigmented nevi
• Progressive hereditary glomerulonephritis without deafness
• Proteus syndrome
• Radial aplasia-thrombocytopenia syndrome
• Radiation chimera
• Renal dysplasia and retinal aplasia
• 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
• Stickler syndrome
• Stunted embryo
• Suspect cystic fibrosis fetus
• Symphalangism-brachydactyly syndrome
• Synotus
• Thalidomide embryopathy syndrome
• Thoracoceloschisis
• Townes syndrome
• Transient mucociliary clearance defect
• Tricho-dento-osseous syndrome
• Trichorhinophalangeal dysplasia type i
• Trichorhinophalangeal syndrome
• Tricho-thiodystrophy
• Triplet monster
• Type iii short rib polydactyly 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
• Weaver syndrome
• Weill-marchesani syndrome
• Wildervanck's syndrome
• Williams syndrome
• Wissler-fanconi syndrome
• Young's syndrome

Applies To

• Congenital malformation syndromes affecting multiple systems, NEC
• Laurence-Moon-Biedl syndrome

Convert 759.89 to ICD-10-CM

ICD-9-CM 759.89 converts approximately to:

• 2013 ICD-10-CM E78.71 Barth syndrome
  Or:
• 2013 ICD-10-CM E78.72 Smith-Lemli-Opitz syndrome
  Or:
• 2013 ICD-10-CM Q87.2 Congenital malformation syndromes predominantly involving limbs
  Or:
• 2013 ICD-10-CM Q87.3 Congenital malformation syndromes involving early overgrowth
  Or:
• 2013 ICD-10-CM Q87.5 Other congenital malformation syndromes with other skeletal changes
  Or:
• 2013 ICD-10-CM Q87.81 Alport syndrome
  Or:
• 2013 ICD-10-CM Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
  Or:
• 2013 ICD-10-CM Q89.8 Other specified congenital malformations

ICD-9-CM Volume 2 Index entries containing back-references to 759.89:

• Abrachiocephalia 759.89
• Abrachiocephalus 759.89
• Absence (organ or part) (complete or partial)
  • heart (congenital) 759.89
    • acquired - see Status, organ replacement
  • organ
    • of Corti (congenital) 744.05
    • or site
      • acquired V45.79
      • 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
    • of Corti (causing impairment of hearing) 744.05
    • or site 759.9
      • specified type NEC 759.89
  • specified type NEC
    • adrenal (gland) 759.1
    • alimentary tract (complete) (partial) 751.8
      • lower 751.5
      • upper 750.8
    • ankle 755.69
    • anus, anal (canal) 751.5
    • aorta, aortic 747.29
      • arch 747.21
    • appendix 751.5
    • arm 755.59
    • artery (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
      • brain 747.81
      • coronary 746.85
      • eye 743.58
      • pulmonary 747.3
      • retinal 743.58
      • umbilical 747.5
    • auditory canal 744.29
      • causing impairment of hearing 744.02
    • bile duct or passage 751.69
    • bladder 753.8
      • neck 753.8
    • bone(s) 756.9
      • arm 755.59
      • face 756.0
      • leg 755.69
      • pelvic girdle 755.69
      • shoulder girdle 755.59
      • skull 756.0
        • with
          • anencephalus 740.0
          • encephalocele 742.0
          • hydrocephalus 742.3
          • with spina bifida (see also Spina bifida) 741.0
          • microcephalus 742.1
    • brain 742.4
    • breast 757.6
    • broad ligament 752.19
    • bronchus 748.3
    • canal of Nuck 752.89
    • cardiac septal closure 745.8
    • carpus 755.59
    • cartilaginous 756.9
    • cecum 751.5
    • cervix 752.49
    • chest (wall) 756.3
    • chin 744.89
    • ciliary body 743.46
    • circulatory system 747.89
    • clavicle 755.51
    • clitoris 752.49
    • coccyx 756.19
    • colon 751.5
    • common duct 751.69
    • connective tissue 756.89
    • cricoid cartilage 748.3
    • cystic duct 751.69
    • diaphragm 756.6
    • digestive organ(s) or tract 751.8
      • lower 751.5
      • upper 750.8
    • duodenum 751.5
    • ear 744.29
      • auricle 744.29
        • causing impairment of hearing 744.02
      • causing impairment of hearing 744.09
      • inner (causing impairment of hearing) 744.05
      • middle, except ossicles 744.03
        • ossicles 744.04
    • ejaculatory duct 752.89
    • endocrine 759.2
    • epiglottis 748.3
    • esophagus 750.4
    • Eustachian tube 744.24
    • eye 743.8
      • lid 743.63
      • muscle 743.69
    • face 744.89
      • bone(s) 756.0
    • fallopian tube 752.19
    • fascia 756.89
    • femur 755.69
    • fibula 755.69
    • finger 755.59
    • foot 755.67
    • fovea centralis 743.55
    • gallbladder 751.69
    • Gartner's duct 752.89
    • gastrointestinal tract 751.8
    • genitalia, genital organ(s)
      • female 752.89
        • external 752.49
        • internal NEC 752.89
      • male 752.89
        • penis 752.69
        • scrotal transposition 752.81
    • genitourinary tract NEC 752.89
    • glottis 748.3
    • hair 757.4
    • hand 755.59
    • heart 746.89
      • valve NEC 746.89
        • pulmonary 746.09
    • hepatic duct 751.69
    • hydatid of Morgagni 752.89
    • hymen 752.49
    • integument 757.8
    • intestine (large) (small) 751.5
      • fixational type 751.4
    • iris 743.46
    • jejunum 751.5
    • joint 755.8
    • kidney 753.3
    • knee 755.64
    • labium (majus) (minus) 752.49
    • labyrinth, membranous 744.05
    • larynx 748.3
    • leg 755.69
    • lens 743.39
    • limb, except reduction deformity 755.8
      • lower 755.69
        • reduction deformity (see also Deformity, reduction, lower limb) 755.30
      • upper 755.59
        • reduction deformity (see also Deformity, reduction, upper limb) 755.20
    • lip 750.26
    • liver 751.69
    • lung (fissure) (lobe) 748.69
    • meatus urinarius 753.8
    • metacarpus 755.59
    • mouth 750.26
    • Müllerian
      • cervix 752.49
      • uterus 752.39
      • vagina 752.49
    • muscle 756.89
      • eye 743.69
    • musculoskeletal system, except limbs 756.9
    • nail 757.5
    • neck 744.89
    • nerve 742.8
      • acoustic 742.8
      • optic 742.8
    • nervous system 742.8
    • nipple 757.6
    • nose 748.1
    • organ NEC 759.89
      • of Corti 744.05
    • osseous meatus (ear) 744.03
    • ovary 752.0
    • oviduct 752.19
    • pancreas 751.7
    • parathyroid 759.2
    • patella 755.64
    • pelvic girdle 755.69
    • penis 752.69
    • pericardium 746.89
    • peripheral vascular system NEC (see also Anomaly, peripheral vascular system) 747.60
    • pharynx 750.29
    • pituitary 759.2
    • prostate 752.89
    • radius 755.59
    • rectum 751.5
    • respiratory system 748.8
    • rib 756.3
    • round ligament 752.89
    • sacrum 756.19
    • salivary duct or gland 750.26
    • scapula 755.59
    • sclera 743.47
    • scrotum 752.89
      • transposition 752.81
    • seminal duct or tract 752.89
    • shoulder girdle 755.59
    • site NEC 759.89
    • skin 757.39
    • skull (bone(s)) 756.0
      • with
        • anencephalus 740.0
        • encephalocele 742.0
        • hydrocephalus 742.3
          • with spina bifida (see also Spina bifida) 741.0
        • microcephalus 742.1
    • specified organ or site NEC 759.89
    • spermatic cord 752.89
    • spinal cord 742.59
    • spine 756.19
    • spleen 759.0
    • sternum 756.3
    • stomach 750.7
    • tarsus 755.67
    • tendon 756.89
    • testis 752.89
    • thorax (wall) 756.3
    • thymus 759.2
    • thyroid (gland) 759.2
      • cartilage 748.3
    • tibia 755.69
    • toe 755.66
    • tongue 750.19
    • trachea (cartilage) 748.3
    • ulna 755.59
    • urachus 753.7
    • ureter 753.4
      • obstructive 753.29
    • urethra 753.8
      • obstructive 753.6
    • urinary tract 753.8
    • uterus (Müllerian) 752.39
    • uvula 750.26
    • vagina 752.49
    • vascular NEC (see also Anomaly, peripheral vascular system) 747.60
      • brain 747.81
    • vas deferens 752.89
    • vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
      • brain 747.81
      • great 747.49
      • portal 747.49
      • pulmonary 747.49
    • vena cava (inferior) (superior) 747.49
    • vertebra 756.19
    • vulva 752.49
• 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 752.43
    • 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) 747.3
    • 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 752.31
    • 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 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) 752.43
  • 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 747.3
    • 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 752.32
  • 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 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