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 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-like hereditary nephritis 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 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 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-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 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 Papillon-Lef 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 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 Synotus Thalidomide embryopathy syndrome Thoracoceloschisis Townes syndrome Transient mucociliary clearance defect Tricho-dento-osseous syndrome Tricho-thiodystrophy 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 | |