- 1001. CONGEN BRONCHIECTASIS
- (UMLS (ICD9CM) C0152239) =Congenital Abnormality; Disease or Syndrome
| - 1051. congenital atelectasis
- [ ] (UMLS (CSP) C0599325) =Pathologic Function ;
|
- 1002. CONGEN CV DIS PREG-UNSP
- [ ] (UMLS (ICD9CM) C0156861) =Disease or Syndrome
| - 1052. congenital biliary tract disorder
- [abnormality present at birth of function, structure, or both of the organs, ducts, and other structures that participate in the secretion, storage, and delivery of bile into the duodenum. ( CSP )] (UMLS (CSP) C0596361) =Congenital Abnormality; Disease or Syndrome =Biliary Tract Disease;
congenital disorder |
- 1003. CONGEN CV DIS-ANTEPARTUM
- [ ] (UMLS (ICD9CM) C0156864) =Disease or Syndrome
| - 1053. congenital blood disorder
- [disorders of the blood and blood forming tissues that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0596362) =Congenital Abnormality; Disease or Syndrome =BLOOD DISEASE NOS;
congenital disorder =ANEMIA HEMOLITIKOA;
congenital erythropoietic porphyria;
congenital blood protein disorder;
perinatal blood group incompatibility;
congenital aplastic anemia;
|
- 1004. CONGEN CV DIS-DEL W P/P
- [ ] (UMLS (ICD9CM) C0156863) =Disease or Syndrome
| - 1054. congenital blood protein disorder
- [blood protein disorders that exist at, and usually before, birth regardless of their causation; blood proteins include but not limited to serum albumin, blood coagulation factors and plasma proteins. ( CSP )] (UMLS (CSP) C0596363) =Disease or Syndrome ;
=blood protein disorder;
congenital blood disorder |
- 1005. CONGEN CV DIS-DELIVERED
- [ ] (UMLS (ICD9CM) C0156862) =Disease or Syndrome
| - 1055. congenital brain disorder
- [pathologic condition existing at, and usually before, birth affecting the brain, which is composed of the intracranial components of the central nervous system. ( CSP )] (UMLS (CSP) C0596364) =Congenital Abnormality ;
=Brain Diseases;
congenital disorder =anencephalus;
hydrocephalus;
micrencephaly;
cerebroatrophic hyperammonemia;
Bourneville's disease;
cerebrohepatorenal syndrome |
- 1006. CONGEN CV DIS-POSTPARTUM
- [ ] (UMLS (ICD9CM) C0156865) =Disease or Syndrome
| - 1056. congenital cardiovascular disorder
- [imperfections or malformations of the cardiovascular system, existing at birth, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C1971810) =Congenital Abnormality; Disease or Syndrome =ASCVD;
congenital disorder =aorta coarctation;
congenital heart disorder;
congenital cardiovascular shunt |
- 1007. CONGEN CYSTIC EYEBALL
- [ ] (UMLS (ICD9CM) C0158543) =Congenital Abnormality; Disease or Syndrome
| - 1057. Congenital cardiovascular disorders complicating pregnancy, childbirth, or the puerperium
- [ ] (UMLS (ICD9CM) C0156860) =Disease or Syndrome
|
- 1008. CONGEN FUSION OF SPINE
- (UMLS (ICD9CM) C0265678) =Congenital Abnormality ;
| - 1058. congenital cardiovascular shunt
- [abnormal, tangled collections of dilated blood vessels that result from congenitally malformed vascular structures in which arterial afferents flow directly into venous efferents without the usual resistance of an intervening capillary bed; these disorders exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0596366) =Congenital Abnormality ;
=congenital cardiovascular disorder;
=Ductus Arteriosus, Patent;
Congenital Arteriovenous Fistula |
- 1009. CONGEN HIP DISLOC, BILAT
- [ ] (UMLS (ICD9CM) C0158713) =Congenital Abnormality
| - 1059. Congenital cataract and lens anomalies
- [ ] (UMLS (ICD9CM) C0158548) =Congenital Abnormality ;
|
- 1010. CONGEN LIMB ANOMALY NEC
- [ ] (UMLS (ICD9CM) C0478072) =Congenital Abnormality ;
| - 1060. CONGENITAL CATARACT NOS
- (UMLS (ICD9CM) C0009691) =Congenital Abnormality ;
|
- 1011. CONGEN LIMB ANOMALY NOS
- [Congenital structural deformities of the upper and lower extremities collectively or unspecified. ( MSH )] (UMLS (ICD9CM) C0206762) =Congenital Abnormality =Aangeboren afw bewegingsapparaat;
=Ectromelia;
Foot Deformities, Congenital;
Hand Deformities, Congenital;
Syndactyly;
Thanatophoric Dysplasia;
Proteus Syndrome;
Polydactyly;
| - 1061. CONGENITAL CHORDEE
- (UMLS (ICD9CM) C0266436) =Congenital Abnormality ;
|
- 1012. CONGEN MITRAL STENOSIS
- [ ] (UMLS (ICD9CM) C0158618) =Congenital Abnormality ;
| - 1062. Congenital cortical and zonular cataract
- [ ] (UMLS (ICD9CM) C0489970) =Congenital Abnormality; Disease or Syndrome
|
- 1013. CONGEN NIGHT BLINDNESS
- [ ] (UMLS (ICD9CM) C1306122) Congenital night blindness =Congenital Abnormality; Disease or Syndrome
| - 1063. CONGENITAL COXA VALGA
- (UMLS (ICD9CM) C0152430) =Congenital Abnormality; Disease or Syndrome
|
- 1014. CONGEN OBST URTROPLV JNC
- [ ] (UMLS (ICD9CM) C0375530) =Congenital Abnormality
| - 1064. CONGENITAL COXA VARA
- (UMLS (ICD9CM) C0152431) =Congenital Abnormality ;
|
- 1015. CONGEN SYPH ENCEPHALITIS
- [ ] (UMLS (ICD9CM) C0153133) =Disease or Syndrome
| - 1065. congenital cranial defect
- [ ] (UMLS (CSP) C0265527) =Congenital Abnormality ;
|
- 1016. CONGEN SYPH MENINGITIS
- [ ] (UMLS (ICD9CM) C0153134) =Disease or Syndrome
| - 1066. CONGENITAL CYSTIC LUNG
- [ ] (UMLS (ICD9CM) C0158641) =Congenital Abnormality ;
|
- 1017. congenic breeding
- [ ] (UMLS (CSP) C0872135) =Organism Function
| - 1067. congenital deafness
- [complete loss of the ability to hear from both ears since birth, regardless of causation. ( CSP )] (UMLS (CSP) C0339789) =Congenital Abnormality; Disease or Syndrome =deafness;
congenital ear disorder =Usher syndrome |
- 1018. congenic transplantation
- [ ] (UMLS (CSP) C1537004) =Therapeutic or Preventive Procedure
| - 1068. Congenital deformities of eyelids
- (UMLS (ICD9CM) C0266572) =Congenital Abnormality ;
|
- 1019. Congenital abnormalities of uterus complicating pregnancy, childbirth, or the puerperium
- [ ] (UMLS (ICD9CM) C0157005) =Congenital Abnormality; Disease or Syndrome
| - 1069. Congenital Deformity of Hip
- (UMLS (NCI) C0265615) =Congenital Abnormality ;
|
- 1020. Congenital Adrenal Gland Disorder
- (UMLS (NCI) C1333142) =Disease or Syndrome ;
| - 1070. Congenital Dental Disorder
- (UMLS (NCI) C0947885) =Congenital Abnormality
|
- 1021. Congenital Adrenal Gland Hypoplasia
- (UMLS (NCI) C0220766) =Congenital Abnormality
| - 1071. congenital dentition disorder
- [disorders of the dental system that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0040427) =Congenital Abnormality =Dental Disorder;
congenital disorder;
Stomatognathic System Abnormalities;
dental disorder =amelogenesis imperfecta;
Dens in Dente;
Dentin Dysplasia;
Dentinogenesis Imperfecta;
Fused Teeth;
SUPERNUMERARY TEETH;
Odontodysplasia;
ANODONTIA |
- 1022. Congenital Alopecia
- (UMLS (NCI) C0265992) =Congenital Abnormality ;
| - 1072. Congenital digestive system anomalies
- [Congenital structural abnormalities of the DIGESTIVE SYSTEM.(MSH)] (UMLS (ICPC) C0266015) (Congenital digestive system anomalies; (194); (115); (116); (104); (105); (106); (108); (119); (133); (130); (122); (123)) Congenital digestive system anomalies =Congenital Abnormality ;
=Aangeboren afwijking spijsvert org; Digestive Diseases =Anus, Imperforate; Barrett Esophagus; biliary atresia; Diaphragmatic Eventration; esophageal atresia; aganglionic megacolon; Intestinal Atresia; Meckel Diverticulum; Caroli's Disease; Gag Reflex Abnormality |
- 1023. CONGENITAL ANEMIA
- [ ] (UMLS (ICD9CM) C0158995) =Disease or Syndrome ;
| - 1073. CONGENITAL DIPLEGIA
- [ ] (UMLS (ICD9CM) C0154695) =Disease or Syndrome ;
|
- 1024. Congenital Angioma
- [A hemangioma present at birth. ( NCI )] (UMLS (NCI) C0235753) =Congenital Abnormality
| - 1074. Congenital dislocation of hip
- [Congenital dislocation of the hip generally includes subluxation of the femoral head, acetabular dysplasia, and complete dislocation of the femoral head from the true acetabulum. This condition occurs in approximately 1 in 1000 live births and is more common in females than in males. ( MSH )] (UMLS (ICD9CM) C0019555) =Congenital Abnormality; Disease or Syndrome =arthropathic;
Aangeboren afw bewegingsapparaat |
- 1025. Congenital anomal resp system
- [Congenital structural abnormalities of the respiratory system.(MSH)] (UMLS (ICPC) C0035238) (Congenital anomal resp system; ARNAS SISTEMAKO SORTZETIKAKO ANOMALIA; Medfodt misdannelse i luftveje; Aangeboren afwijkingen luchtwegen; SYNNYNNAINEN EPAMUODOSTUMA HENGITYSELIMISSA; Anomalie congen syst respir; angeb Missbildung der Atmungsorgane; (108); legzosz. veleszul.rendellen.; Anomalie congenite sistema respir; MEDFODTE FEIL; Malformacoes congenitas; Alt congenitas ap respiratorio; MEDFODDA MISSBILDN I ANDNINGSORGANEN) =Congenital Abnormality; Disease or Syndrome =Aangeboren afwijking spijsvert org; Respiratory Tract Diseases; Diagnosis/Diseases Component; Respiratory =Bronchogenic Cyst; Bronchopulmonary Sequestration; CHOANAL ATRESIA; Cystic Adenomatoid Malformation of Lung, Congenital; Kartagener's Syndrome; Scimitar Syndrome; Tracheobronchomegaly
| - 1075. congenital disorder
- [existing at, and usually before, birth; referring to conditions that are present at birth, regardless of their causation; inborn metabolism disorders are generally not treed here. ( CSP )] (UMLS (CSP) C0242354) =Disease or Syndrome ;
=Disease;
=Congenital hypothyroidism;
DiGeorge Anomaly;
Congenital anomalies of eye;
embryo/fetus disorder;
Prader Willi syndrome;
Congenital anomalies of the integument;
congenital dentition disorder;
familial hypogonadism with anosmia;
RSH Syndrome;
Beuren syndrome;
congenital skeletal disorder;
congenital infection;
congenital nervous system disorder;
congenital kidney disorder;
congenital reproductive system disorder;
congenital biliary tract disorder;
congenital blood disorder;
congenital brain disorder;
congenital ear disorder;
congenital gastrointestinal disorder;
congenital oral/facial/cranial defect;
congenital hepatic porphyria;
congenital respiratory disorder;
congenital muscle disorder;
congenital cardiovascular disorder |
- 1026. Congenital anomalies
- [Any abnormality, anatomical or biochemical, evident at birth or during the neonatal period.(NCI)] (UMLS (ICPC) C0000768) (Congenital anomalies; LISERI SISTEMAKO SORTZETIKO ANOMALIA; Medfodt anomali i fordoj system; Aangeboren afwijkingen zenuwst; SYNNYNNAISET EPAMUODOSTUMAT; Anomalies congenitales; angeborene Missbildung Nervensystem; (108); veleszuletett rendellenesseg; Anomalie congenite; MEDFODTE FEIL/MANGLER; Malformacoes congenitas; Anomalias congenitas; MEDFODDA MISSBILDNINGAR) =Congenital Abnormality
| - 1076. Congenital Disorder of Natural Immunity
- (UMLS (NCI) C1333144) =Disease or Syndrome ;
|
- 1027. Congenital anomalies female genital
- (UMLS (ICPC) C0266365) (Congenital anomalies female genital; EMAKUMEZKO GENITALEKO SORTZETIKO ANOMALIA; Medfodt misdan kvin genitalier; Aangeboren afw gesl org) (vrouw); NAISEN SUKUELINTEN SYNNYNNAISET EPAMUODOSTUMAT; Anomalies congenitales gen femin; angeb Missbild weibl Genitale/Brust; (108); noi genit. veleszul. rendellen.; Anomalie congenite genit femm; MEDFODTE FEIL KVINNELIG GENITALIA; Malformacoes congenitas; An congenitas ap genit femenino; MEDFODDA MISSBILDN I KVINNLIGA GENITALIA) =Congenital Abnormality ;
=FEMALE GENITAL SYSTEM (INCLUDING BREAST); Diagnosis/Diseases Component | - 1077. congenital ear disorder
- [impairment of health or a condition of abnormal functioning in the sense organ for hearing and equilibrium that exist at, and usually before, birth regardless of causation. ( CSP )] (UMLS (CSP) C0596367) =Disease or Syndrome ;
=DISORDER OF EAR NOS;
congenital disorder =congenital deafness;
|
- 1028. Congenital anomalies of ear
- (UMLS (ICPC) C0266589) (Congenital anomalies of ear; BELARRIAN SORTZETIKO ANOMALIA; Medfodt misdannelse af ore; Aangeboren afwijkingen oor; KORVAN SYNNYNNAISET EPAMUODOSTUMAT; Anomalies congenitales oreille; angeborene Missbildungen des Ohres; (108); ful veleszul. rendellenessege; Anomalie congenite dell'orecchio; MEDFODTE FEIL; Malformacoes congenitas ouvido; Anomalias congenitas oido; MEDFODDA ORONMISSBILDNINGAR) =Congenital Abnormality ;
=auris; Diagnosis/Diseases Component | - 1078. CONGENITAL ECTOPIC LENS
- [Congenital displacement of the lens resulting from defective zonule formation. ( MSH )] (UMLS (ICD9CM) C0013581) =Congenital Abnormality ;
=Congenital anomalies of eye;
Lens Subluxation |
- 1029. Congenital anomalies of ear causing impairment of hearing
- (UMLS (ICD9CM) C0266592) =Congenital Abnormality; Disease or Syndrome
| - 1079. Congenital Epilepsy
- (UMLS (NCI) C0854109) =Disease or Syndrome
|
- 1030. Congenital anomalies of ear, face, and neck
- [ ] (UMLS (ICD9CM) C0158581) =Congenital Abnormality; Disease or Syndrome
| - 1080. Congenital Epulis
- (UMLS (NCI) C0376319) =Congenital Abnormality
|
- 1031. Congenital anomalies of eye
- [absence of or defects in structures of the eye that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (ICD9CM) C0015393) =Congenital Abnormality ;
=Aangeboren afwijking spijsvert org;
Disorder of eye, unspecified;
congenital disorder;
=microphthalmia;
congenital vision disorder;
ANIRIDIA;
Anophthalmos;
BLEPHAROPHIMOSIS;
Coloboma;
CONGENITAL ECTOPIC LENS;
Buphthalmos;
microphthalmia;
Retinal Dysplasia;
| - 1081. congenital erythropoietic porphyria
- [autosomal recessive porphyria characterized by splenomegaly, photosensitivity, hemolytic anemia, and the appearance of red urine in early infancy; results from increased synthesis of uroporphyrinogen I relative to uroporphyrinogen III in bone marrow normoblasts. ( CSP )] (UMLS (CSP) C0162530) =Disease or Syndrome =Genetic Condition;
DIS PORPHYRIN METABOLISM;
Skin Diseases, Genetic;
congenital blood disorder |
- 1032. Congenital anomalies of eyelids, lacrimal system, and orbit
- [ ] (UMLS (ICD9CM) C0158572) =Disease or Syndrome ;
| - 1082. Congenital Eyelid Ptosis
- (UMLS (NCI) C0266573) =Congenital Abnormality ;
|
- 1033. Congenital anomalies of genital organs
- [ ] (UMLS (ICD9CM) C0158687) =Congenital Abnormality ;
| - 1083. congenital facial defect
- [ ] (UMLS (CSP) C0266617) =Congenital Abnormality ;
|
- 1034. Congenital anomalies of mother
- (UMLS (ICPC) C0497444) (Congenital anomalies of mother; HAURDUNAL.KONPLIKAZIOA AMAREN SORTZETIKO ANOMALIAK (*); Medfodt misd moders arsag t kompl; Zwang compl aangeb afw moeder; AIDIN * SYNNYNNAISET EPAMUODOSTUMAT; Anomalies congenitales de la mere; angeb Missbild Mutter: SchwKomplik; (108); terh-t bef. anyai velesz.rendell.; Anomalie cong della madre; MEDFODTE FEIL HOS MOREN SOM KOMPL; Lesoes congenitas da mae; Anomalias congenitas madre; MEDFODDA MISSBILDN HOS MOR) Cong anomalies of mother =Congenital Abnormality =PREGNANCY, CHILDBEARING, FAMILY PLANNING; Diagnosis/Diseases Component
| - 1084. Congenital Fibrosarcoma
- [A fibrosarcoma, occurring in infants and young children, sharing identical morphologic features with adult fibrosarcoma. The prognosis is generally much more favorable than for adult fibrosarcoma, and it rarely metastasizes. It usually affects the superficial and deep soft tissues of the extremities. The majority of infantile fibrosarcomas carry the t(12;15)(p13;q26) translocation. ( NCI )] (UMLS (NCI) C0334459) =Neoplastic Process
|
- 1035. Congenital anomalies of other specified sites of peripheral vascular system
- [ ] (UMLS (ICD9CM) C0375521) =Congenital Abnormality
| - 1085. Congenital fistula of lip
- [ ] (UMLS (ICD9CM) C0158670) =Congenital Abnormality ;
|
- 1036. Congenital anomalies of posterior segment
- [ ] (UMLS (ICD9CM) C0439001) =Congenital Abnormality
| - 1086. congenital gastrointestinal disorder
- [disorders of the gastrointestinal system that exist at, and usually before, birth regardless of their causation; refers to diseases in the digestive structures stretching from the mouth to anus, but does not include the accessory glandular organs. ( CSP )] (UMLS (CSP) C0596368) =Congenital Abnormality ;
=Gastrointestinal Diseases;
congenital disorder =aganglionic megacolon;
acrodermatitis enteropathica |
- 1037. Congenital anomalies of the integument
- [structural abnormalities of the skin that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (ICD9CM) C0037268) =Congenital Abnormality; Disease or Syndrome =Aangeboren afwijking spijsvert org;
Cutaneous Disorder;
Skin Diseases, Genetic;
congenital disorder =cutis elastica;
acantholysis bullosa;
hereditary hyperbilirubinemia;
congenital ichthyosis;
Darier's disease;
pseudoxanthoma elasticum;
UP/MPCM;
Aldrich syndrome;
Angioma Pigmentosum Atrophicum;
acrodermatitis enteropathica;
acrodermatitis;
CONG ECTODERMAL DYSPLAS;
cutis elastica;
acantholysis bullosa;
Ichthyosis;
Incontinentia Pigmenti;
Poikiloderma Congenitale;
pseudoxanthoma elasticum;
SCLEREMA NEONATORUM;
Angioma Pigmentosum Atrophicum;
Nevus Flammeus;
Dyskeratosis Congenita | - 1087. Congenital Genitourinary Abnormality
- [Congenital structural abnormalities of the UROGENITAL SYSTEM in either the male or the female. ( MSH )] (UMLS (NCI) C0042063) =Congenital Abnormality; Disease or Syndrome =Aangeboren afwijking spijsvert org;
DISEASES OF THE GENITOURINARY SYSTEM =BLADDER EXSTROPHY;
Cryptorch/niet ingedaalde testis;
EPISPADIAS;
polycystic kidney;
Hereditary Nephritis;
sex differentiation disorder;
WAGR Syndrome;
Multicystic Dysplastic Kidney;
Hipospadias |
- 1038. Congenital anomalies urinary tract
- (UMLS (ICPC) C0158698) (Congenital anomalies urinary tract; GERNU TRAKTOKO SORTZETIKO ANOMALIA; Medfodt misdannelse i urinveje; Aangeboren afwijkingen urinewegen; VIRTSATEIDEN SYNNYNNAISET EPAMUODOSTUMAT; Anomalie congen syst urinaire; angeborene Missbild Nieren/Harnwege; (108); urologiai veleszul.rendelleness.; Anomalie congenite tratto urin; MEDFODTE FEIL; Malf congenitas tracto urinario; An congenitas del tracto urin; MEDFODDA MISSBILDN I URINVAGARNA) =Congenital Abnormality ;
=Urologic; Diagnosis/Diseases Component | - 1088. Congenital genu recurvatum and bowing of long bones of leg
- (UMLS (ICD9CM) C0431946) =Congenital Abnormality ;
|
- 1039. Congenital anomaly of gastrointestinal vessel
- [ ] (UMLS (ICD9CM) C0375518) =Congenital Abnormality
| - 1089. Congenital Hallux Valgus
- (UMLS (NCI) C0265656) =Congenital Abnormality ;
|
- 1040. Congenital anomaly of Lower limb vessel
- [ ] (UMLS (ICD9CM) C0375520) =Congenital Abnormality
| - 1090. Congenital Hamartoma
- (UMLS (NCI) C1302749) =Congenital Abnormality ;
|
- 1041. Congenital anomaly of lung, unspecified
- [ ] (UMLS (ICD9CM) C0158644) =Congenital Abnormality ;
| - 1091. CONGENITAL HEART BLOCK
- (UMLS (ICD9CM) C0149530) =Disease or Syndrome
|
- 1042. Congenital anomaly of middle ear, except ossicles
- (UMLS (ICD9CM) C0431468) =Congenital Abnormality ;
| - 1092. congenital heart disorder
- [imperfections or malformations of the heart, existing at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0152021) =Disease or Syndrome =CARDIAC DISORDERS;
congenital cardiovascular disorder =congenital heart septum defect;
tetralogy of Fallot;
COMPL TRANSPOS GREAT VES;
Alagille syndrome;
Holt Oram syndrome;
|
- 1043. Congenital anomaly of Renal vessel
- [ ] (UMLS (ICD9CM) C0302468) =Congenital Abnormality
| - 1093. congenital heart septum defect
- [defects in the cardiac septa, resulting in abnormal communications between the opposite chambers of the heart that exist at, and usually before, birth regardless of their causation. ( CSP )] (UMLS (CSP) C0018816) =Congenital Abnormality; Disease or Syndrome =CONG HEART ANOMALY NOS;
congenital heart disorder =asymmetric septal hypertrophy;
Aortopulmonary Septal Defect;
ENDOCARD CUSHION DEF NOS;
atrial septal defect;
Heart Septal Defects, Ventricular |
- 1044. Congenital anomaly of spinal vessel
- [ ] (UMLS (ICD9CM) C0375522) =Congenital Abnormality
| - 1094. CONGENITAL HEMIPLEGIA
- [ ] (UMLS (ICD9CM) C0270805) =Disease or Syndrome
|
- 1045. Congenital anomaly of the peripheral vascular system, unspecified site
- [ ] (UMLS (ICD9CM) C0340797) =Congenital Abnormality
| - 1095. congenital hepatic porphyria
- [disorders characterized by the liver excessively producing porphyrins or their precursors, arising from abnormalities in the regulation of the porphyrin-heme pathway existing at, and usually before, birth regardless of causation; porphyria, acute intermittent and porphyria cutanea tarda are types of hepatic porphyria. ( CSP )] (UMLS (CSP) C0687708) =Disease or Syndrome ;
=Hepatic Disorder;
DIS PORPHYRIN METABOLISM;
congenital disorder;
|
- 1046. Congenital anomaly of upper limb vessel
- [ ] (UMLS (ICD9CM) C0375519) =Congenital Abnormality
| - 1096. CONGENITAL HIATUS HERNIA
- [ ] (UMLS (ICD9CM) C0158674) =Congenital Abnormality; Disease or Syndrome
|
- 1047. Congenital anomaly/birth defect
- (UMLS (HL7) C1546948) =Idea or Concept =Event Consequence;
| - 1097. CONGENITAL HYDROCELE
- [ ] (UMLS (ICD9CM) C0159015) =Congenital Abnormality
|
- 1048. CONGENITAL APHAKIA
- (UMLS (ICD9CM) C0152422) =Congenital Abnormality ;
| - 1098. CONGENITAL HYDROCEPHALUS
- (UMLS (ICD9CM) C0020256) =Congenital Abnormality
|
- 1049. congenital aplastic anemia
- [familial or idiopathic form, usually fatal; Fanconi's anemia presents before age 10, marked by microcephaly, skin discolorations, and sexual and mental retardation. ( CSP )] (UMLS (CSP) C0702159) =Disease or Syndrome ;
=Anemia, Aplastic;
congenital blood disorder | - 1099. congenital hyperammonemia type II
- [ ] (UMLS (CSP) C0543537) =Congenital Abnormality; Disease or Syndrome
|
- 1050. Congenital Arteriovenous Fistula
- [structural anomaly present at birth which allows direct passage of blood from an artery to a vein. ( CSP )] (UMLS (NCI) C0332965) =Congenital Abnormality ;
=congenital cardiovascular shunt;
| - 1100. congenital hyperbilirubinemia
- [ ] (UMLS (CSP) C0238077) =Congenital Abnormality; Disease or Syndrome
|
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