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759.89 - Other Specified Congenital Anomalies

The ICD 9 Code for Other specified congenital anomalies is listed as 759.89.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
ICD 9 CM Field Value
Diagnosis Code: 759.89
Long Description: Other specified congenital anomalies
Short Description: Specfied cong anomal NEC
Chapter: Congenital Anomalies
Block: Other and unspecified congenital anomalies (759-759)
Related Descriptions: Aarskog syndrome
Aase syndrome
Abnormal fetal duplication
Abnormal fetus
Acardiac monster
Acardiacus anceps
Acquired and/or congenital pulmonary valve atresia
Acquired mucociliary clearance defect
Adams-Oliver syndrome
Allemann's syndrome
Alport syndrome-like hereditary nephritis
Alstrom syndrome
Andersen Tawil syndrome
Angelman syndrome
Anomalies of umbilicus
Arteriohepatic dysplasia
Asymmetric crying face association
Autositic monster
Bannayan syndrome
Bardet-Biedl 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
Branchiooculofacial syndrome
Cardio-acral-facial syndrome
Cardio-facio-cutaneous syndrome
Carpenter's syndrome
Caudal dysplasia sequence
Celosomial monster
Cerebro-costo-mandibular syndrome
Cerebro-oculo-facio-skeletal syndrome
Cerebrofacial dysplasia
Child syndrome
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
Currarino triad
Cyclops hypognathus
Cylindrical embryo
Danon disease
De Lange syndrome
Double monster
Duhamel's syndrome
Dyggve-Melchior-Clausen syndrome
Dysmorphic sialidosis, congenital form
Ectopic fetus
Epstein syndrome
Escobar syndrome
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-Chaudhry-Moss syndrome
Grebe syndrome
Grob's syndrome
Hanhart's syndrome
Hecht syndrome
Hemihypertrophy of muscle
Hereditary nephritis
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
Loeys-Dietz syndrome
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome
Marchesani syndrome
Marden Walker syndrome
Marfanoid joint hypermobility syndrome
Marshall syndrome
Marshall-Smith syndrome
Maternal phenylketonuria 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 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 (aplasia cutis, skin tags, eye & brain defects)
Oculo-palato-digital syndrome
Oculodento-osseous dysplasia
Oculodento-osseous dysplasia - mild type
Oculodento-osseous dysplasia - severe type
Oculodentodigital syndrome
Oral-facial-digital syndrome
Oromandibular-limb hypogenesis spectrum
Osteochondrodysplasia with osteopetrosis
Oto-onycho-peroneal syndrome
Oto-palato-digital syndrome, type I
Oto-palato-digital syndrome, type II
Otocephalic syndrome
Otospondylomegaepiphyseal dysplasia
Pallister-Hall syndrome
Parasitic monster
Pena-Shokeir phenotype
Pentalogy of Cantrell
PIBIDS syndrome, photosensitivity with IBIDS
Pili torti-deafness syndrome
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 coloboma syndrome
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
Thalidomide embryopathy syndrome
Townes syndrome
Transient mucociliary clearance defect
Tricho-dento-osseous syndrome
Trichorhinophalangeal dysplasia type I
Trichorhinophalangeal syndrome
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
ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD-10-CM Code: E78.71 - Barth syndrome (approximate)
ICD-10-CM Code: E78.72 - Smith-Lemli-Opitz syndrome (approximate)
ICD-10-CM Code: Q87.2 - Congenital malformation syndromes predominantly involving limbs (approximate)
ICD-10-CM Code: Q87.3 - Congenital malformation syndromes involving early overgrowth (approximate)
ICD-10-CM Code: Q87.5 - Other congenital malformation syndromes with other skeletal changes (approximate)
ICD-10-CM Code: Q87.81 - Alport syndrome (approximate)
ICD-10-CM Code: Q87.89 - Other specified congenital malformation syndromes, not elsewhere classified (approximate)
ICD-10-CM Code: Q89.8 - Other specified congenital malformations (approximate)
ICD-9-CM Siblings (same level / similar specificity) of 759.89:
759.81 - Prader-Willi syndrome
759.82 - Marfan syndrome
759.83 - Fragile X syndrome