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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Congential Anomalies 740-759 > Other And Unspecified Congenital Anomalies 759.* >

2008 ICD-9-CM Diagnosis 759.89

Other specified congenital anomalies

  • 759.89 is a specific code that can be used to specify a diagnosis
  • 759.89 contains 167 index entries
  • View the ICD-9-CM Volume 1 759.* hierarchy

759.89 also known as:

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


Index entries containing 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
    • 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
    • site NEC 759.89
    • specified organ or site NEC 759.89
Atresia, atretic (congenital) 759.89Barth syndrome 759.89
Beckwith (-Wiedemann) syndrome 759.89
Biedl-Bardet syndrome 759.89
Biemond's syndrome (obesity, polydactyly, and mental retardation) 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)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
  • 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) 759.89Fibromatosis 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) 759.89Hyperekplexia 759.89
Hyperexplexia 759.89
Hypoplasia, hypoplasis 759.89Joubert 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
  • double aortic arch 747.21
  • ductus
  • fetal
    • circulation 747.83
    • form of cervix (uteri) 752.49
    • hemoglobin (hereditary) ("Swiss variety") 282.7
    • pulmonary hypertension 747.83
  • foramen
  • Gartner's duct 752.41
  • hemoglobin, fetal (hereditary) (HPFH) 282.7
  • hyaloid
  • 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
  • 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
  • omphalomesenteric duct 751.0
  • organ or site NEC - see Anomaly, specified type NEC
  • ostium
  • ovarian rests in fallopian tube 752.19
  • pancreatic tissue in intestinal tract 751.5
  • primary (deciduous)
  • pulmonary hypertension 747.83
  • pupillary membrane 743.46
  • right aortic arch 747.21
  • sinus
    • urogenitalis 752.89
    • venosus with imperfect incorporation in right auricle 747.49
  • thymus (gland) 254.8
  • 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) 759.89Pseudo-Turner's syndrome 759.89
Rubinstein-Taybi's syndrome (brachydactylia, short stature and mental retardation) 759.89
Rud's syndrome (mental deficiency, epilepsy, and infantilism) 759.89
Russell's dwarf (uterine dwarfism and craniofacial dysostosis) 759.89
Russell (-Silver) syndrome (congenital hemihypertrophy and short stature) 759.89
Seborrhea, seborrheic 706.3
  • nigricans 759.89
Seckel's syndrome 759.89
Sick 799.9
  • cilia syndrome 759.89
Silver's syndrome (congenital hemihypertrophy and short stature 759.89
Sirenomelia 759.89
Smith-Lemli-Opitz syndrome (cerebrohepatorenal syndrome) 759.89
Stickler syndrome 759.89
Stiff-baby 759.89
Sympus 759.89
Syndrome - see also Disease
  • Alagille 759.89
  • Alport's (hereditary hematuria-nephropathy-deafness) 759.89
  • Angelman 759.89
  • Bardet-Biedl (obesity, polydactyly, and mental retardation) 759.89
  • Barth 759.89
  • Beckwith (-Wiedemann) 759.89
  • Biedl-Bardet (obesity, polydactyly, and mental retardation) 759.89
  • Biemond's (obesity, polydactyly, and mental retardation) 759.89
  • Borjeson-Forssman-Lehmann 759.89
  • Brachman-de Lange (Amsterdam dwarf, mental retardation, and brachycephaly) 759.89
  • Carpenter's 759.89
  • cerebrohepatorenal 759.89
  • CHARGE association 759.89
  • Cockayne's (microencephaly and dwarfism) 759.89
  • Coffin-Lowry 759.89
  • congenital
    • affecting more than one system 759.7
      • specified type NEC 759.89
    • muscular hypertrophy-cerebral 759.89
  • de Lange's (Amsterdam dwarf, mental retardation, and brachycephaly) (Cornelia) 759.89
  • Fraser's 759.89
  • Freeman-Sheldon 759.89
  • Gillespie's (dysplasia oculodentodigitalis) 759.89
  • Gorlin-Chaudhry-Moss 759.89
  • inverted Marfan's 759.89
  • Joubert 759.89
  • Kabuki 759.89
  • Klippel-Trenaunay 759.89
  • Laurence-Moon (-Bardet)-Biedl (obesity, polydactyly, and mental retardation) 759.89
  • Marchesani (-Weill) (brachymorphism and ectopia lentis) 759.89
  • Menkes' 759.89
    • glutamic acid 759.89
    • maple syrup (urine) disease 270.3
  • Meyer-Schwickerath and Weyers (dysplasia oculodentodigitalis) 759.89
  • microphthalmos (congenital) 759.89
  • Mieten's 759.89
  • Mohr's (types I and II) 759.89
  • Neill Dingwall (microencephaly and dwarfism) 759.89
  • Noonan's 759.89
  • oral-facial-digital 759.89
  • ordigitofacial 759.89
  • otopalatodigital 759.89
  • Papillon-Léage and Psaume (orodigitofacial dysostosis) 759.89
  • pseudo-Turner's 759.89
  • Rubinstein-Taybi's (brachydactylia, short stature, and mental retardation) 759.89
  • Rud's (mental deficiency, epilepsy, and infantilism) 759.89
  • Russell (-Silver) (congenital hemihypertrophy and short stature) 759.89
  • Seckel's 759.89
  • sick
    • cilia 759.89
  • Silver's (congenital hemihypertrophy and short stature) 759.89
  • Smith-Lemli-Opitz (cerebrohepatorenal syndrome) 759.89
  • spherophakia-brachymorphia 759.89
  • Stickler 759.89
  • stiff-baby 759.89
  • Taybi's (otopalatodigital) 759.89
  • Ullrich-Feichtiger 759.89
  • VATER 759.89
  • Weill-Marchesani (brachymorphism and ectopia lentis) 759.89
  • "whistling face" (craniocarpotarsal dystrophy) 759.89
Synophthalmus 759.89
Taybi's syndrome (otopalatodigital) 759.89
Teratencephalus 759.89
Thoracogastroschisis (congenital) 759.89
Ullrich-Feichtiger syndrome 759.89
VATER syndrome 759.89
Weill-Marchesani syndrome (brachymorphism and ectopia lentis) 759.89
"Whistling face" syndrome (craniocarpotarsal dystrophy) 759.89