Specific code 2014 ICD-9-CM Diagnosis Code 759.89
Other specified congenital anomalies
  • Billable Code
  • 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.
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
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
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: