Specific code 2012 ICD-9-CM Diagnosis Code 759.89
Other specified congenital anomalies
  • Short description: Specfied cong anomal NEC.
  • 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).
  • You are viewing the 2012 version of ICD-9-CM 759.89.
  • More recent version(s) of ICD-9-CM 759.89: 2013 2014 2015.
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
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 2012 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.