2011 ICD-9-CM Diagnosis Code 759.89 : Other specified congenital anomalies

Home > 2011 ICD-9-CM Diagnosis Codes > Congenital Anomalies 740-759 > Other and unspecified congenital anomalies 759-

2011 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 2011 version of ICD-9-CM 759.89.
More recent version(s) of ICD-9-CM 759.89: 2012 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
- specified type NEC
  - adrenal (gland) 759.1
  - alimentary tract (complete) (partial) 751.8
    - lower 751.5
    - upper 750.8
  - ankle 755.69
  - anus, anal (canal) 751.5
  - aorta, aortic 747.29
    - arch 747.21
  - appendix 751.5
  - arm 755.59
  - artery (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
    - coronary 746.85
    - eye 743.58
    - pulmonary 747.3
    - retinal 743.58
    - umbilical 747.5
  - auditory canal 744.29
    - causing impairment of hearing 744.02
  - bile duct or passage 751.69
  - bladder 753.8
    - neck 753.8
  - bone(s) 756.9
    - arm 755.59
    - face 756.0
    - leg 755.69
    - pelvic girdle 755.69
    - shoulder girdle 755.59
    - skull 756.0
      - with
        anencephalus 740.0
        encephalocele 742.0
        hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
        microcephalus 742.1
  - brain 742.4
  - breast 757.6
  - broad ligament 752.19
  - bronchus 748.3
  - canal of Nuck 752.89
  - cardiac septal closure 745.8
  - carpus 755.59
  - cartilaginous 756.9
  - cecum 751.5
  - cervix 752.49
  - chest (wall) 756.3
  - chin 744.89
  - ciliary body 743.46
  - circulatory system 747.89
  - clavicle 755.51
  - clitoris 752.49
  - coccyx 756.19
  - colon 751.5
  - common duct 751.69
  - connective tissue 756.89
  - cricoid cartilage 748.3
  - cystic duct 751.69
  - diaphragm 756.6
  - digestive organ(s) or tract 751.8
    - lower 751.5
    - upper 750.8
  - duodenum 751.5
  - ear 744.29
    - auricle 744.29
      - causing impairment of hearing 744.02
    - causing impairment of hearing 744.09
    - inner (causing impairment of hearing) 744.05
    - middle, except ossicles 744.03
      - ossicles 744.04
  - ejaculatory duct 752.89
  - endocrine 759.2
  - epiglottis 748.3
  - esophagus 750.4
  - Eustachian tube 744.24
  - eye 743.8
    - lid 743.63
    - muscle 743.69
  - face 744.89
    - bone(s) 756.0
  - fallopian tube 752.19
  - fascia 756.89
  - femur 755.69
  - fibula 755.69
  - finger 755.59
  - foot 755.67
  - fovea centralis 743.55
  - gallbladder 751.69
  - Gartner's duct 752.89
  - gastrointestinal tract 751.8
  - genitalia, genital organ(s)
    - female 752.89
      - external 752.49
      - internal NEC 752.89
    - male 752.89
      - penis 752.69
      - scrotal transposition 752.81
  - genitourinary tract NEC 752.89
  - glottis 748.3
  - hair 757.4
  - hand 755.59
  - heart 746.89
    - valve NEC 746.89
      - pulmonary 746.09
  - hepatic duct 751.69
  - hydatid of Morgagni 752.89
  - hymen 752.49
  - integument 757.8
  - intestine (large) (small) 751.5
    - fixational type 751.4
  - iris 743.46
  - jejunum 751.5
  - joint 755.8
  - kidney 753.3
  - knee 755.64
  - labium (majus) (minus) 752.49
  - labyrinth, membranous 744.05
  - larynx 748.3
  - leg 755.69
  - lens 743.39
  - limb, except reduction deformity 755.8
    - lower 755.69
      - reduction deformity (see also Deformity, reduction, lower limb) 755.30
    - upper 755.59
      - reduction deformity (see also Deformity, reduction, upper limb) 755.20
  - lip 750.26
  - liver 751.69
  - lung (fissure) (lobe) 748.69
  - meatus urinarius 753.8
  - metacarpus 755.59
  - mouth 750.26
  - Müllerian
    - cervix 752.49
    - uterus 752.39
    - vagina 752.49
  - muscle 756.89
    - eye 743.69
  - musculoskeletal system, except limbs 756.9
  - nail 757.5
  - neck 744.89
  - nerve 742.8
    - acoustic 742.8
    - optic 742.8
  - nervous system 742.8
  - nipple 757.6
  - nose 748.1
  - organ NEC 759.89
    - of Corti 744.05
  - osseous meatus (ear) 744.03
  - ovary 752.0
  - oviduct 752.19
  - pancreas 751.7
  - parathyroid 759.2
  - patella 755.64
  - pelvic girdle 755.69
  - penis 752.69
  - pericardium 746.89
  - peripheral vascular system NEC (see also Anomaly, peripheral vascular system) 747.60
  - pharynx 750.29
  - pituitary 759.2
  - prostate 752.89
  - radius 755.59
  - rectum 751.5
  - respiratory system 748.8
  - rib 756.3
  - round ligament 752.89
  - sacrum 756.19
  - salivary duct or gland 750.26
  - scapula 755.59
  - sclera 743.47
  - scrotum 752.89
    - transposition 752.81
  - seminal duct or tract 752.89
  - shoulder girdle 755.59
  - site NEC 759.89
  - skin 757.39
  - skull (bone(s)) 756.0
    - with
      - anencephalus 740.0
      - encephalocele 742.0
      - hydrocephalus 742.3
        with spina bifida (see also Spina bifida) 741.0
      - microcephalus 742.1
  - specified organ or site NEC 759.89
  - spermatic cord 752.89
  - spinal cord 742.59
  - spine 756.19
  - spleen 759.0
  - sternum 756.3
  - stomach 750.7
  - tarsus 755.67
  - tendon 756.89
  - testis 752.89
  - thorax (wall) 756.3
  - thymus 759.2
  - thyroid (gland) 759.2
    - cartilage 748.3
  - tibia 755.69
  - toe 755.66
  - tongue 750.19
  - trachea (cartilage) 748.3
  - ulna 755.59
  - urachus 753.7
  - ureter 753.4
    - obstructive 753.29
  - urethra 753.8
    - obstructive 753.6
  - urinary tract 753.8
  - uterus (Müllerian) 752.39
  - uvula 750.26
  - vagina 752.49
  - vascular NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
  - vas deferens 752.89
  - vein(s) (peripheral) NEC (see also Anomaly, peripheral vascular system) 747.60
    - brain 747.81
    - great 747.49
    - portal 747.49
    - pulmonary 747.49
  - vena cava (inferior) (superior) 747.49
  - vertebra 756.19
  - vulva 752.49
Atresia, atretic (congenital) 759.89
- alimentary organ or tract NEC 751.8
  - lower 751.2
  - upper 750.8
- 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
- aortic (orifice) (valve) 746.89
  - arch 747.11
- aqueduct of Sylvius 742.3
  - with spina bifida (see also Spina bifida) 741.0
- artery NEC (see also Atresia, blood vessel) 747.60
  - cerebral 747.81
  - coronary 746.85
  - eye 743.58
  - pulmonary 747.3
  - umbilical 747.5
- auditory canal (external) 744.02
- bile, biliary duct (common) or passage 751.61
  - acquired (see also Obstruction, biliary) 576.2
- bladder (neck) 753.6
- blood vessel (peripheral) NEC 747.60
  - cerebral 747.81
  - gastrointestinal 747.61
  - lower limb 747.64
  - pulmonary artery 747.3
  - renal 747.62
  - spinal 747.82
  - upper limb 747.63
- bronchus 748.3
- canal, ear 744.02
- cardiac
  - valve 746.89
    - aortic 746.89
    - mitral 746.89
    - pulmonary 746.01
    - tricuspid 746.1
- cecum 751.2
- 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
- choana 748.0
- colon 751.2
- cystic duct 751.61
  - acquired 575.8
    - with obstruction (see also Obstruction, gallbladder) 575.2
- digestive organs NEC 751.8
- duodenum 751.1
- ear canal 744.02
- ejaculatory duct 752.89
- epiglottis 748.3
- esophagus 750.3
- Eustachian tube 744.24
- fallopian tube (acquired) 628.2
  - congenital 752.19
- follicular cyst 620.0
- 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
- gallbladder 751.69
- genital organ
  - external
    - female 752.49
    - male NEC 752.89
      - penis 752.69
  - internal
    - female 752.89
    - male 752.89
- glottis 748.3
- gullet 750.3
- heart
  - valve NEC 746.89
    - aortic 746.89
    - mitral 746.89
    - pulmonary 746.01
    - tricuspid 746.1
- hymen 752.42
  - acquired 623.3
  - postinfective 623.3
- ileum 751.1
- intestine (small) 751.1
  - large 751.2
- iris, filtration angle (see also Buphthalmia) 743.20
- jejunum 751.1
- kidney 753.3
- lacrimal, apparatus 743.65
  - acquired - see Stenosis, lacrimal
- larynx 748.3
- ligament, broad 752.19
- lung 748.5
- meatus urinarius 753.6
- 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
- nasolacrimal duct 743.65
- nasopharynx 748.8
- nose, nostril 748.0
  - acquired 738.0
- organ or site NEC - see Anomaly, specified type NEC
- osseous meatus (ear) 744.03
- oviduct (acquired) 628.2
  - congenital 752.19
- parotid duct 750.23
  - acquired 527.8
- pulmonary (artery) 747.3
  - valve 746.01
  - vein 747.49
- pulmonic 746.01
- pupil 743.46
- rectum 751.2
- salivary duct or gland 750.23
  - acquired 527.8
- sublingual duct 750.23
  - acquired 527.8
- submaxillary duct or gland 750.23
  - acquired 527.8
- trachea 748.3
- tricuspid valve 746.1
- ureter 753.29
- ureteropelvic junction 753.21
- ureterovesical orifice 753.22
- urethra (valvular) 753.6
- urinary tract NEC 753.29
- uterus 752.31
  - acquired 621.8
- vagina (acquired) 623.2
  - congenital (total) (partial) 752.45
  - postgonococcal (old) 098.2
  - postinfectional 623.2
  - senile 623.2
- vascular NEC (see also Atresia, blood vessel) 747.60
  - cerebral 747.81
- vas deferens 752.89
- vein NEC (see also Atresia, blood vessel) 747.60
  - cardiac 746.89
  - great 747.49
  - portal 747.49
  - pulmonary 747.49
- vena cava (inferior) (superior) 747.49
- vesicourethral orifice 753.6
- vulva 752.49
  - acquired 624.8
Barth syndrome 759.89
Beckwith (-Wiedemann) syndrome 759.89
Biedl-Bardet syndrome 759.89
Biemond's syndrome (obesity, polydactyly, and mental retardation) 759.89
Birt-Hogg-Dube syndrome 759.89
Brachman-de Lange syndrome (Amsterdam dwarf, mental retardation, and brachycephaly) 759.89
Brachymorphism and ectopia lentis 759.89
Bruck-de Lange disease or syndrome (Amsterdam dwart, mental retardation, 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, mental retardation, and brachycephaly) 759.89
Cyclencephaly 759.89
Cyclopia, cyclops 759.89
Cyllosoma 759.89
Cyst (mucus) (retention) (serous) (simple)
- congenital NEC 759.89
  - adrenal glands 759.1
  - epiglottis 748.3
  - esophagus 750.4
  - fallopian tube 752.11
  - kidney 753.10
    - multiple 753.19
    - single 753.11
  - larynx 748.3
  - liver 751.62
  - lung 748.4
  - mediastinum 748.8
  - ovary 752.0
  - oviduct 752.11
  - pancreas 751.7
  - periurethral (tissue) 753.8
  - prepuce NEC 752.69
    - penis 752.69
  - sublingual 750.26
  - submaxillary gland 750.26
  - thymus (gland) 759.2
  - tongue 750.19
  - ureterovesical orifice 753.4
  - vulva 752.41
- umbilicus 759.89
Deformity 738.9
- multiple, congenital NEC 759.7
  - specified type NEC 759.89
de Lange's syndrome (Amsterdam dwarf, mental retardation, and brachycephaly) 759.89
Disease, diseased - see also Syndrome
- Bruck-de Lange (Amsterdam dwarf, mental retardation, and brachycephaly) 759.89
- Cockayne's (microcephaly and dwarfism) 759.89
- Kok 759.89
- polycystic (congenital) 759.89
  - kidney or renal 753.12
    - adult type (APKD) 753.13
    - autosomal dominant 753.13
    - autosomal recessive 753.14
    - childhood type (CPKD) 753.14
    - infantile type 753.14
  - liver or hepatic 751.62
  - lung or pulmonary 518.89
    - congenital 748.4
  - ovary, ovaries 256.4
  - spleen 759.0
- 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
- ACTH syndrome 255.0
- adrenal gland 759.1
- anus 751.5
- auricular beats 427.61
- beats 427.60
- bladder 753.5
- bone and cartilage in lung 748.69
- brain 742.4
- breast tissue 757.6
- cardiac 746.87
- cerebral 742.4
- cordis 746.87
- endometrium 617.9
- gallbladder 751.69
- gastric mucosa 750.7
- gestation - see Pregnancy, ectopic
- heart 746.87
- 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
- lens 743.37
- lentis 743.37
- mole - see Pregnancy, ectopic
- organ or site NEC - see Malposition, congenital
- ovary 752.0
- pancreas, pancreatic tissue 751.7
- pregnancy - see Pregnancy, ectopic
- pupil 364.75
- renal 753.3
- sebaceous glands of mouth 750.26
- secretion
  - ACTH 255.0
  - adrenal hormone 259.3
  - adrenalin 259.3
  - adrenocorticotropin 255.0
  - antidiuretic hormone (ADH) 259.3
  - epinephrine 259.3
  - hormone NEC 259.3
  - norepinephrine 259.3
  - pituitary (posterior) 259.3
- spleen 759.0
- testis 752.51
- thyroid 759.2
- ureter 753.4
- ventricular beats 427.69
- vesicae 753.5
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
- cranial 756.0
Hyperekplexia 759.89
Hyperexplexia 759.89
Hypoplasia, hypoplasis 759.89
- adrenal (gland) 759.1
- alimentary tract 751.8
  - lower 751.2
  - upper 750.8
- anus, anal (canal) 751.2
- aorta 747.22
- 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
- appendix 751.2
- areola 757.6
- arm (see also Absence, arm, congenital) 755.20
- artery (congenital) (peripheral) 747.60
  - brain 747.81
  - cerebral 747.81
  - coronary 746.85
  - gastrointestinal 747.61
  - lower limb 747.64
  - pulmonary 747.3
  - renal 747.62
  - retinal 743.58
  - specified NEC 747.69
  - spinal 747.82
  - umbilical 747.5
  - upper limb 747.63
- auditory canal 744.29
  - causing impairment of hearing 744.02
- biliary duct (common) or passage 751.61
- bladder 753.8
- bone NEC 756.9
  - face 756.0
  - malar 756.0
  - mandible 524.04
    - alveolar 524.74
  - marrow 284.9
    - acquired (secondary) 284.89
    - congenital 284.09
    - idiopathic 284.9
  - maxilla 524.03
    - alveolar 524.73
  - skull (see also Hypoplasia, skull) 756.0
- brain 742.1
  - gyri 742.2
  - specified part 742.2
- breast (areola) 611.82
- bronchus (tree) 748.3
- cardiac 746.89
  - valve - see Hypoplasia, heart, valve
  - vein 746.89
- carpus (see also Absence, carpal, congenital) 755.28
- cartilaginous 756.9
- cecum 751.2
- cementum 520.4
  - hereditary 520.5
- cephalic 742.1
- cerebellum 742.2
- cervix (uteri) 752.43
- chin 524.06
- clavicle 755.51
- coccyx 756.19
- colon 751.2
- corpus callosum 742.2
- cricoid cartilage 748.3
- dermal, focal (Goltz) 757.39
- digestive organ(s) or tract NEC 751.8
  - lower 751.2
  - upper 750.8
- ear 744.29
  - auricle 744.23
  - lobe 744.29
  - middle, except ossicles 744.03
    - ossicles 744.04
  - ossicles 744.04
- enamel of teeth (neonatal) (postnatal) (prenatal) 520.4
  - hereditary 520.5
- endocrine (gland) NEC 759.2
- endometrium 621.8
- epididymis 752.89
- epiglottis 748.3
- erythroid, congenital 284.01
- erythropoietic, chronic acquired 284.81
- esophagus 750.3
- Eustachian tube 744.24
- eye (see also Microphthalmos) 743.10
  - lid 743.62
- face 744.89
  - bone(s) 756.0
- fallopian tube 752.19
- femur (see also Absence, femur, congenital) 755.34
- fibula (see also Absence, fibula, congenital) 755.37
- finger (see also Absence, finger, congenital) 755.29
- focal dermal 757.39
- foot 755.31
- gallbladder 751.69
- genitalia, genital organ(s)
  - female 752.89
    - external 752.49
    - internal NEC 752.89
  - in adiposogenital dystrophy 253.8
  - male 752.89
    - penis 752.69
- glottis 748.3
- hair 757.4
- hand 755.21
- heart 746.89
  - left (complex) (syndrome) 746.7
  - valve NEC 746.89
    - pulmonary 746.01
- humerus (see also Absence, humerus, congenital) 755.24
- hymen 752.49
- intestine (small) 751.1
  - large 751.2
- iris 743.46
- jaw 524.09
- kidney(s) 753.0
- labium (majus) (minus) 752.49
- labyrinth, membranous 744.05
- lacrimal duct (apparatus) 743.65
- larynx 748.3
- 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
- liver 751.69
- lung (lobe) 748.5
- mammary (areolar) 611.82
- mandibular 524.04
  - alveolar 524.74
  - unilateral condylar 526.89
- maxillary 524.03
  - alveolar 524.73
- medullary 284.9
- megakaryocytic 287.30
- metacarpus (see also Absence, metacarpal, congenital) 755.28
- metatarsus (see also Absence, metatarsal, congenital) 755.38
- muscle 756.89
  - eye 743.69
- myocardium (congenital) (Uhl's anomaly) 746.84
- nail(s) 757.5
- nasolacrimal duct 743.65
- nervous system NEC 742.8
- neural 742.8
- nose, nasal 748.1
- ophthalmic (see also Microphthalmos) 743.10
- optic nerve 377.43
- organ
  - of Corti 744.05
  - or site NEC - see Anomaly, by site
- osseous meatus (ear) 744.03
- ovary 752.0
- oviduct 752.19
- pancreas 751.7
- parathyroid (gland) 759.2
- parotid gland 750.26
- patella 755.64
- pelvis, pelvic girdle 755.69
- penis 752.69
- peripheral vascular system (congenital) NEC 747.60
  - gastrointestinal 747.61
  - lower limb 747.64
  - renal 747.62
  - specified NEC 747.69
  - spinal 747.82
  - upper limb 747.63
- pituitary (gland) 759.2
- pulmonary 748.5
  - arteriovenous 747.3
  - artery 747.3
  - valve 746.01
- punctum lacrimale 743.65
- radioulnar (see also Absence, radius, congenital, with ulna) 755.25
- radius (see also Absence, radius, congenital) 755.26
- rectum 751.2
- respiratory system NEC 748.9
- rib 756.3
- sacrum 756.19
- scapula 755.59
- shoulder girdle 755.59
- skin 757.39
- skull (bone) 756.0
  - with
    - anencephalus 740.0
    - encephalocele 742.0
    - hydrocephalus 742.3
      - with spina bifida (see also Spina bifida) 741.0
    - microcephalus 742.1
- spinal (cord) (ventral horn cell) 742.59
  - vessel 747.82
- spine 756.19
- spleen 759.0
- sternum 756.3
- tarsus (see also Absence, tarsal, congenital) 755.38
- testis, testicle 752.89
- thymus (gland) 279.11
- thyroid (gland) 243
  - cartilage 748.3
- tibiofibular (see also Absence, tibia, congenital, with fibula) 755.35
- toe (see also Absence, toe, congenital) 755.39
- tongue 750.16
- trachea (cartilage) (rings) 748.3
- Turner's (tooth) 520.4
- ulna (see also Absence, ulna, congenital) 755.27
- umbilical artery 747.5
- ureter 753.29
- uterus 752.32
- vagina 752.45
- vascular (peripheral) NEC (see also Hypoplasia, peripheral vascular system) 747.60
  - brain 747.81
- vein(s) (peripheral) NEC (see also Hypoplasia, peripheral vascular system) 747.60
  - brain 747.81
  - cardiac 746.89
  - great 747.49
  - portal 747.49
  - pulmonary 747.49
- vena cava (inferior) (superior) 747.49
- vertebra 756.19
- vulva 752.49
- zonule (ciliary) 743.39
- zygoma 738.12
Joubert syndrome 759.89
Kabuki syndrome 759.89
Klippel-Trenaunay syndrome 759.89
Laurence-Moon-Biedl syndrome (obesity, polydactyly, and mental retardation) 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
- anal membrane 751.2
- arteria stapedia 744.04
- atrioventricular canal 745.69
- bloody ejaculate 792.2
- branchial cleft 744.41
- bulbus cordis in left ventricle 745.8
- canal of Cloquet 743.51
- capsule (opaque) 743.51
- cilioretinal artery or vein 743.51
- cloaca 751.5
- communication - see Fistula, congenital
- convolutions
  - aortic arch 747.21
  - fallopian tube 752.19
  - oviduct 752.19
  - uterine tube 752.19
- double aortic arch 747.21
- ductus
  - arteriosus 747.0
  - Botalli 747.0
- fetal
  - circulation 747.83
  - form of cervix (uteri) 752.49
  - hemoglobin (hereditary) ("Swiss variety") 282.7
  - pulmonary hypertension 747.83
- foramen
  - Botalli 745.5
  - ovale 745.5
- Gartner's duct 752.41
- hemoglobin, fetal (hereditary) (HPFH) 282.7
- hyaloid
  - artery (generally incomplete) 743.51
  - system 743.51
- hymen (tag)
  - in pregnancy or childbirth 654.8
    - causing obstructed labor 660.2
- lanugo 757.4
- left
  - posterior cardinal vein 747.49
  - root with right arch of aorta 747.21
  - superior vena cava 747.49
- Meckel's diverticulum 751.0
- mesonephric duct 752.89
  - fallopian tube 752.11
- mucosal disease (middle ear) (with posterior or superior marginal perforation of ear drum) 382.2
- nail(s), anomalous 757.5
- occiput, anterior or posterior 660.3
  - fetus or newborn 763.1