Specific code 2015 ICD-9-CM Diagnosis Code 759.89
Other specified congenital anomalies
  • 2015
  • Billable Thru Sept 30/2015
  • Non-Billable On/After Oct 1/2015

  • ICD-9-CM 759.89 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 759.89 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Convert to ICD-10-CM: 759.89 converts approximately to:
  • 2015/16 ICD-10-CM E78.71 Barth syndrome
    Or:
  • 2015/16 ICD-10-CM E78.72 Smith-Lemli-Opitz syndrome
    Or:
  • 2015/16 ICD-10-CM Q87.2 Congenital malformation syndromes predominantly involving limbs
    Or:
  • 2015/16 ICD-10-CM Q87.3 Congenital malformation syndromes involving early overgrowth
    Or:
  • 2015/16 ICD-10-CM Q87.5 Other congenital malformation syndromes with other skeletal changes
    Or:
  • 2015/16 ICD-10-CM Q87.81 Alport syndrome
    Or:
  • 2015/16 ICD-10-CM Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    Or:
  • 2015/16 ICD-10-CM Q89.8 Other specified congenital malformations
Approximate Synonyms
  • 3-Methylglutaconic aciduria type 2
  • 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
  • Alagille syndrome
  • Allemann's syndrome
  • Alport syndrome
  • Alport syndrome-like hereditary nephritis
  • Alports syndrome
  • Alstrom syndrome
  • Anadidymus
  • Andersen Tawil syndrome
  • Angelman syndrome
  • Anomalies of umbilicus
  • Arteriohepatic dysplasia
  • Asymmetric crying face association
  • Atretocephalus
  • Autositic monster
  • Bannayan syndrome
  • Bardet-Biedl syndrome
  • Barth syndrome
  • Basal cell nevus syndrome
  • Beckwith Wiedemann 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
  • Charge association
  • Charge 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 hemihypertrophy
  • 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 syndrome
  • Gorlin-Chaudhry-Moss syndrome
  • Grebe syndrome
  • Grob's syndrome
  • Hanhart's syndrome
  • Hecht syndrome
  • Hemihypertrophy of muscle
  • Hereditary diffuse crescentic glomerulonephritis
  • Hereditary diffuse endocapillary proliferative glomerulonephritis
  • Hereditary diffuse membranous glomerulonephritis
  • Hereditary diffuse mesangial proliferative glomerulonephritis
  • Hereditary diffuse mesangiocapillary glomerulonephritis
  • Hereditary focal and segmental glomerular lesions
  • Hereditary mesangiocapillary glomerulonephritis, type 2
  • Hereditary minor glomerular abnormality
  • Hereditary nephritis
  • Hereditary nephropathy
  • Hereditary nephropathy w crescentic glomerulonephritis
  • Hereditary nephropathy w dense deposit disease
  • Hereditary nephropathy w endocapillary proliferative glomerulonephritis
  • Hereditary nephropathy w focal segmental glomerular lesions
  • Hereditary nephropathy w membranoproliferative glomerulonephritis, type 1
  • Hereditary nephropathy w membranoproliferative glomerulonephritis, type 3
  • Hereditary nephropathy w membranous glomerulonephritis
  • Hereditary nephropathy w mesangial proliferative glomerulonephritis
  • Hereditary nephropathy w minimal change lesion
  • Hereditary nephropathy with membranoproliferative glomerulonephritis, type 3
  • 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
  • Kabuki make-up syndrome
  • Kabuki syndrome
  • Kenny syndrome
  • Klippel Trenaunay Weber 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 syndrome
  • 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
  • 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
  • Vater association
  • 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
Clinical Information
  • 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
Applies To
  • Congenital malformation syndromes affecting multiple systems, NEC
  • Laurence-Moon-Biedl syndrome
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
  • Atresia, atretic (congenital) 759.89
    • 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
    • aqueduct of Sylvius 742.3
      • with spina bifida (see also Spina bifida) 741.0
    • auditory canal (external) 744.02
    • bile, biliary duct (common) or passage 751.61
      • acquired (see also Obstruction, biliary) 576.2
    • 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
    • cystic duct 751.61
      • acquired 575.8
        • with obstruction (see also Obstruction, gallbladder) 575.2
    • digestive organs NEC 751.8
    • 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
    • iris, filtration angle (see also Buphthalmia) 743.20
    • lacrimal, apparatus 743.65
      • acquired - see Stenosis, lacrimal
    • 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
    • organ or site NEC - see Anomaly, specified type NEC
    • vascular NEC (see also Atresia, blood vessel) 747.60
    • vena cava (inferior) (superior) 747.49
    • vesicourethral orifice 753.6
  • 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)
    • 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
    • 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
    • bone and cartilage in lung 748.69
    • gestation - see Pregnancy, ectopic
    • 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
    • mole - see Pregnancy, ectopic
    • organ or site NEC - see Malposition, congenital
    • pancreas, pancreatic tissue 751.7
    • pregnancy - see Pregnancy, ectopic
    • sebaceous glands of mouth 750.26
  • 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
  • Hyperekplexia 759.89
  • Hyperexplexia 759.89
  • Hypoplasia, hypoplasis 759.89
    • angiolymphoid, with eosinophilia (ALHE) 228.01
    • 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
    • arm (see also Absence, arm, congenital) 755.20
    • biliary duct (common) or passage 751.61
    • cardiac 746.89
      • valve - see Hypoplasia, heart, valve
      • vein 746.89
    • carpus (see also Absence, carpal, congenital) 755.28
    • enamel of teeth (neonatal) (postnatal) (prenatal) 520.4
    • endocrine (gland) NEC 759.2
    • erythropoietic, chronic acquired 284.81
    • femur (see also Absence, femur, congenital) 755.34
    • fibula (see also Absence, fibula, congenital) 755.37
    • finger (see also Absence, finger, congenital) 755.29
    • humerus (see also Absence, humerus, congenital) 755.24
    • lacrimal duct (apparatus) 743.65
    • 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
    • metacarpus (see also Absence, metacarpal, congenital) 755.28
    • metatarsus (see also Absence, metatarsal, congenital) 755.38
    • myocardium (congenital) (Uhl's anomaly) 746.84
    • ophthalmic (see also Microphthalmos) 743.10
    • organ
      • of Corti 744.05
      • or site NEC - see Anomaly, by site
    • parathyroid (gland) 759.2
    • radioulnar (see also Absence, radius, congenital, with ulna) 755.25
    • radius (see also Absence, radius, congenital) 755.26
    • respiratory system NEC 748.9
    • tarsus (see also Absence, tarsal, congenital) 755.38
    • tibiofibular (see also Absence, tibia, congenital, with fibula) 755.35
    • toe (see also Absence, toe, congenital) 755.39
    • trachea (cartilage) (rings) 748.3
    • ulna (see also Absence, ulna, congenital) 755.27
    • vascular (peripheral) NEC (see also Hypoplasia, peripheral vascular system) 747.60
    • vena cava (inferior) (superior) 747.49
  • 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-Léage and Psaume syndrome (orodigitofacial dysostosis) 759.89
  • Persistence, persistent (congenital) 759.89
    • bulbus cordis in left ventricle 745.8
    • cilioretinal artery or vein 743.51
    • communication - see Fistula, congenital
    • fetal
      • circulation 747.83
      • form of cervix (uteri) 752.49
      • hemoglobin (hereditary) ("Swiss variety") 282.7
      • pulmonary hypertension 747.83
    • hemoglobin, fetal (hereditary) (HPFH) 282.7
    • hymen (tag)
      • in pregnancy or childbirth 654.8
        • causing obstructed labor 660.2
    • left
      • posterior cardinal vein 747.49
      • root with right arch of aorta 747.21
      • superior vena cava 747.49
    • Meckel's diverticulum 751.0
    • mucosal disease (middle ear) (with posterior or superior marginal perforation of ear drum) 382.2
    • occiput, anterior or posterior 660.3
    • omphalomesenteric duct 751.0
    • organ or site NEC - see Anomaly, specified type NEC
    • ovarian rests in fallopian tube 752.19
    • pancreatic tissue in intestinal tract 751.5
    • primary (deciduous)
    • Rhesus (Rh) titer (see also Complications, transfusion) 999.70
    • sinus
      • urogenitalis 752.89
      • venosus with imperfect incorporation in right auricle 747.49
    • truncus arteriosus or communis 745.0
    • tunica vasculosa lentis 743.39
  • Podencephalus 759.89
  • Polycystic (congenital) (disease) 759.89
    • degeneration, kidney - see Polycystic, kidney
  • 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
      • congenital central alveolar hypoventilation 327.25
      • facial diplegia 352.6
      • 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-Léage 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
    • 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
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 759.89 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2015 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.