Specific code 2006 ICD-9-CM Diagnosis Code 759.89
Other specified congenital anomalies
  • Short description: SPECFIED CONG ANOMAL NEC.
  • ICD-9-CM 759.89 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • 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 2006 version of ICD-9-CM 759.89.
  • More recent version(s) of ICD-9-CM 759.89: 2007 2008 2009 2010 2011 2012 2013 2014.
Disease 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
  • Allemann's syndrome
  • Alport syndrome
  • Alport syndrome-like hereditary nephritis
  • Alports syndrome
  • Alstrom syndrome
  • Anadidymus
  • Andersen Tawil 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
  • 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 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
  • 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 to ICD-10-CM: 759.89 converts approximately to:
  • 2014 ICD-10-CM E78.71 Barth syndrome
    Or:
  • 2014 ICD-10-CM E78.72 Smith-Lemli-Opitz syndrome
    Or:
  • 2014 ICD-10-CM Q87.2 Congenital malformation syndromes predominantly involving limbs
    Or:
  • 2014 ICD-10-CM Q87.3 Congenital malformation syndromes involving early overgrowth
    Or:
  • 2014 ICD-10-CM Q87.5 Other congenital malformation syndromes with other skeletal changes
    Or:
  • 2014 ICD-10-CM Q87.81 Alport syndrome
    Or:
  • 2014 ICD-10-CM Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    Or:
  • 2014 ICD-10-CM Q89.8 Other specified congenital malformations
ICD-9-CM Volume 2 Index entries containing back-references to 759.89: