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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
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C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CO COA COB COC COD COE COF COG COH COI COK COL COM CON COO COP COQ COR COS COT COU COV COW COX COY COZ
selected terms: 1,975
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901. Confederated Salish & Kootenai Tribes of the Flath
(UMLS (HL7) C1554273) =Population Group =NativeEntityContiguous;
951. CONG CNTRL HYPOVENT SYND
[ ] (UMLS (ICD9CM) C1561866) Congenital central alveolar hypoventilation syndrome;
=Disease or Syndrome
902. Confederated Tribes and Bands of the Yakama Indian
(UMLS (HL7) C1554282) =Population Group =NativeEntityContiguous;
952. CONG CORNEA OPAC AFF VIS
[ ] (UMLS (ICD9CM) C0158557) =Congenital Abnormality ;
903. Confederated Tribes of the Chehalis Reservation, W
(UMLS (HL7) C1554274) =Population Group =NativeEntityContiguous;
953. CONG CORNEAL OPACIT NEC
[ ] (UMLS (ICD9CM) C0158558) =Congenital Abnormality ;
904. Confederated Tribes of the Colville Reservation, W
(UMLS (HL7) C1554275) =Population Group =NativeEntityContiguous;
954. CONG CYSTIC LIVER DIS
[ ] (UMLS (ICD9CM) C0158683) =Congenital Abnormality; Disease or Syndrome
905. Confederated Tribes of the Coos, Lower Umpqua and
(UMLS (HL7) C1554276) =Population Group =NativeEntityContiguous;
955. CONG CYTOMEGALOVIRUS INF
[ ] (UMLS (ICD9CM) C0158945) =Congenital Abnormality
906. Confederated Tribes of the Goshute Reservation, Ne
(UMLS (HL7) C1554277) =Population Group =NativeEntityContiguous;
956. CONG DEF CLOT FACTOR NEC
(UMLS (ICD9CM) C0009699) =Disease or Syndrome ;
907. Confederated Tribes of the Grand Ronde Community o
(UMLS (HL7) C1554278) =Population Group =NativeEntityContiguous;
957. CONG DEFORMITY-CLAVICLE
[ ] (UMLS (ICD9CM) C0158760) =Congenital Abnormality ;
908. Confederated Tribes of the Siletz Reservation, Ore
(UMLS (HL7) C1554279) =Population Group =NativeEntityContiguous;
958. CONG ECTODERMAL DYSPLAS
[A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita. ( MSH )] (UMLS (ICD9CM) C0013575) =Congenital Abnormality; Disease or Syndrome =Abnormalities, Multiple;
Sex Chromosome Abnormalities;
Congenital anomalies of the integument;
=CHONDROECTODERM DYSPLAS;
focal dermal hypoplasia;
Neurocutaneous Syndromes;
909. Confederated Tribes of the Umatilla Reservation, O
(UMLS (HL7) C1554280) =Population Group =NativeEntityContiguous;
959. CONG ELEVATION-SCAPULA
(UMLS (ICD9CM) C0152438) =Congenital Abnormality
910. Confederated Tribes of the Warm Springs Reservatio
(UMLS (HL7) C1554281) =Population Group =NativeEntityContiguous;
960. CONG ESOPH FISTULA/ATRES
(UMLS (ICD9CM) C0009733) =Congenital Abnormality; Disease or Syndrome
911. Conference
[Conference; a prearranged meeting for consultation or exchange of information or discussion, especially one with a formal agenda. ( NCI )] (UMLS (NCI) C0086047) =Human-caused Phenomenon or Process
961. CONG FACE/NECK ANOM NEC
[ ] (UMLS (ICD9CM) C0477992) =Congenital Abnormality
912. Confidence Interval
[A range of values for a variable of interest, e.g., a rate, constructed so that this range has a specified probability of including the true value of the variable. ( MSH )] (UMLS (NCI) C0009667) =Quantitative Concept ;
962. CONG FACE/NECK ANOM NOS
[ ] (UMLS (ICD9CM) C0869095) Unspecified congenital anomalies of face and neck =Congenital Abnormality; Disease or Syndrome
913. Confidence Limit
(UMLS (NCI) C0237530) =Quantitative Concept ;
963. CONG FACTOR VIII DIORD
[classic hemophilia resulting from a deficiency of factor VIII; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. ( CSP )] (UMLS (ICD9CM) C0019069) =Disease or Syndrome ;
=blood coagulation disorder;
HEMORRHAGIC COND NOS;
Genetic Condition;
Coagulation Protein Disorders
914. confidentiality
[privacy of information and its protection against unauthorized disclosure. ( CSP )] (UMLS (CSP) C0009669) =Idea or Concept ;
=human rights;
health related legal
964. CONG FACTOR XI DISORDER
[A deficiency of blood coagulation factor XI (known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia. (Dorland, 27th ed) ( MSH )] (UMLS (ICD9CM) C0015523) =Disease or Syndrome =HEMORRHAGIC COND NOS;
Coagulation Protein Disorders
915. Confidentiality
(UMLS (HL7) C1553801) =Intellectual Product =CodeSystem;
=ConfidentialityByAccessKind;
ConfidentialityByInfoType;
ConfidentialityModifiers;
965. CONG FISSURE OF TONGUE
(UMLS (ICD9CM) C0040412) =Disease or Syndrome =Tongue Diseases;
916. Confidentiality code
(UMLS (HL7) C1547595) =Intellectual Product =HL7 Vocabulary Version 2.5;
=AIDS patient;
Employee;
Alcohol/drug treatment patient;
HIV(+) patient;
Psychiatric patient;
Restricted;
Usual control;
Unwed mother;
Very restricted;
Very important person or celebrity;
966. CONG FOLD/CYST POST EYE
[ ] (UMLS (ICD9CM) C0158567) =Congenital Abnormality ;
917. ConfidentialityByAccessKind
[By accessing subject / role and relationship based rights (These concepts are mutually exclusive, one and only one is required for a valid confidentiality coding.) ( HL7V3.0 )] (UMLS (HL7) C1698715) =Qualitative Concept ;
=Confidentiality;
=restricted;
normal;
clinician;
individual;
low;
business;
very restricted
967. CONG FOOT DEFORM NEC
[ ] (UMLS (ICD9CM) C0158729) =Congenital Abnormality
918. ConfidentialityByInfoType
[By information type, only for service catalog entries (multiples allowed). Not to be used with actual patient data! ( HL7V3.0 )] (UMLS (HL7) C1698716) =Qualitative Concept ;
=Confidentiality;
=HIV related;
psychiatry relate;
substance abuse related;
sexual and domestic violence related;
968. CONG GENU RECURVATUM
(UMLS (ICD9CM) C0152235) =Congenital Abnormality ;
919. ConfidentialityModifiers
[Modifiers of role based access rights (multiple allowed) ( HL7V3.0 )] (UMLS (HL7) C1699284) =Qualitative Concept =Confidentiality;
=sensitive;
celebrity;
taboo;
969. CONG HEART ANOMALY NEC
[ ] (UMLS (ICD9CM) C0477999) =Congenital Abnormality
920. Configuring
(UMLS (HL7) C1550004) =Idea or Concept =Equipment state;
970. CONG HEART ANOMALY NOS
[Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life. ( MSH )] (UMLS (ICD9CM) C0018798) =Congenital Abnormality ;
=CARDIAC DISORDERS;
Aangeboren afw hartvaatstelsel =aorta coarctation;
COR TRIATRIATUM;
Coronary Vessel Anomalies;
Crisscross Heart;
Dextrocardia;
Ductus Arteriosus, Patent;
EBSTEIN'S ANOMALY;
Eisenmenger Complex;
congenital heart septum defect;
Levocardia;
tetralogy of Fallot;
COMPL TRANSPOS GREAT VES;
COMMON TRUNCUS;
HYPOPLAS LEFT HEART SYND;
Tricuspid Atresia;
Arrhythmogenic Right Ventricular Dysplasia;
921. Confirm first
[Confirmation with Contact Person prior to making any substitutions has or will occur. ( HL7V3.0 )] (UMLS (HL7) C1555535) =Idea or Concept =Conditional;
971. CONG HERED MUSC DYSTRPHY
(UMLS (ICD9CM) C0699741) =Disease or Syndrome
922. confirmation
[Respond with exceptions, completion, and modification with detail (as above), and send positive confirmations even if no modifications are being made. ( HL7V3.0 )] (UMLS (HL7) C1611825) =Idea or Concept =ResponseLevel;
972. CONG HIP DEFORMITY NEC
[ ] (UMLS (ICD9CM) C0029557) =Congenital Abnormality ;
923. Confirmation
[Having been established or verified. ( NCI )] (UMLS (NCI) C0750484) Confirmatory;
Confirmed;
=Idea or Concept
973. CONG HIP DISLOC W SUBLUX
[ ] (UMLS (ICD9CM) C0158716) =Congenital Abnormality
924. Confirmed but inactive
(UMLS (HL7) C1547324) =Idea or Concept =Allergy Clinical Status;
974. CONG HIP DISLOC, UNILAT
(UMLS (ICD9CM) C0009702) =Congenital Abnormality ;
925. Confirmed or verified
(UMLS (HL7) C1547321) =Idea or Concept =Allergy Clinical Status;
975. CONG HIP SUBLUX, BILAT
[ ] (UMLS (ICD9CM) C0158715) =Congenital Abnormality
926. Conflagration in other and unspecified building or structure
[ ] (UMLS (ICD9CM) C0261627) =Natural Phenomenon or Process
976. CONG HIP SUBLUX, UNILAT
[ ] (UMLS (ICD9CM) C1261276) Congenital subluxation of hip, unilateral =Congenital Abnormality ;
927. Conflagration in private dwelling
[ ] (UMLS (ICD9CM) C0261620) =Injury or Poisoning
977. CONG HYPOGAMMAGLOBULINEM
[ ] (UMLS (ICD9CM) C1457897) Congenital hypogammaglobulinemia;
=Disease or Syndrome ;
928. Conflagration not in building or structure
[ ] (UMLS (ICD9CM) C0261634) =Phenomenon or Process
978. CONG KNEE DEFORMITY
[ ] (UMLS (ICD9CM) C0158767) =Congenital Abnormality ;
929. conflict
[internal individual struggle resulting from incompatible or opposing needs, drives, or external and internal demands; in group interactions, competitive or opposing action of incompatibles: antagonistic state or action (as of divergent ideas, interests, or persons). ( CSP )] (UMLS (CSP) C0009671) =Individual Behavior ;
=psychology;
979. CONG KNEE DISLOCATION
[ ] (UMLS (ICD9CM) C0158718) =Congenital Abnormality
930. Confocal Microscopy
[A system of (usually) epifluorescence light microscopy in which a fine laser beam of light is scanned over the object through the objective lens. The technique is particularly good at rejecting light from outside the plane of focus and so produces higher effective resolution than is normally achieved. ( NCI )] (UMLS (NCI) C0242842) =Laboratory Procedure ;
980. CONG MACROGLOSSIA
(UMLS (ICD9CM) C0009677) =Congenital Abnormality ;
931. confocal scanning microscopy
[indirect imaging technique which uses a sharply focused light source (typically a laser) to excite fluors or otherwise visualize the specimen one point at a time; 2 or 3 dimensional likenesses are then reconstructed by computer; relatively noninvasive, applicable to thick sections and living tissue. ( CSP )] (UMLS (CSP) C0242841) =Laboratory Procedure ;
=microscopy;
981. CONG MACULAR CHANGE-EYE
[ ] (UMLS (ICD9CM) C0158568) =Disease or Syndrome ;
932. Conformal
[any of the spatial arrangements of a molecule that can be obtained by rotation of the atoms about a single bond. ( CSP )] (UMLS (NCI) C0026377) =Molecular Function; Spatial Concept =stereochemistry;
=molecular dynamics
982. CONG MITRAL INSUFFICIENC
[ ] (UMLS (ICD9CM) C0158619) =Congenital Abnormality; Disease or Syndrome
933. Confucian
(UMLS (HL7) C1549422) =Idea or Concept =religion;
983. CONG OBST URETEROVES JNC
[ ] (UMLS (ICD9CM) C0375531) =Congenital Abnormality
934. Confucianism
[A school of thought and set of moral, ethical, and political teachings usually considered to be founded by Confucius in 6th-5th century B.C. China. (from Cambridge Dictionary of Philosophy, 1995) ( MSH )] (UMLS (HL7) C0337700) =Idea or Concept ;
=Religious Affiliation;
984. CONG POSTURAL DEFORMITY
[ ] (UMLS (ICD9CM) C0158712) =Congenital Abnormality
935. Confused
(UMLS (HL7) C1547301) =Intellectual Product =Precaution Code;
985. CONG PULMON VALVE STENOS
[ ] (UMLS (ICD9CM) C0162164) =Congenital Abnormality ;
936. confused flour beetle
[ ] (UMLS (CSP) C0598191) =Invertebrate
986. CONG PYLORIC STENOSIS
[Narrowing of the pyloric canal due to HYPERTROPHY of the surrounding circular muscle. It is usually seen in infants or young children. ( MSH )] (UMLS (ICD9CM) C0700639) =Congenital Abnormality; Disease or Syndrome
937. Confusion
[Confusion; a mental state characterized by a lack of clear and orderly thought and behavior. ( NCI )] (UMLS (NCI) C0009676) =Mental or Behavioral Dysfunction ;
=Neurobehavioral Manifestations;
=delirious
987. CONG RETINAL CHANGES NEC
[ ] (UMLS (ICD9CM) C0029729) =Disease or Syndrome
938. CONFUSIONAL AROUSALS
(UMLS (ICD9CM) C0752295) =Mental or Behavioral Dysfunction ;
988. CONG SALIVARY FISTULA
[ ] (UMLS (ICD9CM) C0158669) =Congenital Abnormality; Disease or Syndrome
939. CONG ABN UTER PREG-UNSP
[ ] (UMLS (ICD9CM) C0157006) =Congenital Abnormality ;
989. CONG SKIN PIGMENT ANOMAL
(UMLS (ICD9CM) C0009726) =Congenital Abnormality ;
940. CONG ABN UTER-DEL W P/P
[ ] (UMLS (ICD9CM) C0157008) =Congenital Abnormality; Disease or Syndrome
990. CONG SKULL/FACE/JAW DEF
(UMLS (ICD9CM) C0432068) =Congenital Abnormality ;
941. CONG ABSENCE EXT EAR
[ ] (UMLS (ICD9CM) C0702139) =Congenital Abnormality ;
991. CONG SUBAORTIC STENOSIS
[ ] (UMLS (ICD9CM) C0158621) =Congenital Abnormality ;
942. CONG ADHESIONS OF TONGUE
[ ] (UMLS (ICD9CM) C0158664) =Congenital Abnormality; Disease or Syndrome
992. CONG TOT/SUBTOT CATARACT
[ ] (UMLS (ICD9CM) C0158552) =Congenital Abnormality ;
943. CONG ANOM OF AORTA NEC
[ ] (UMLS (ICD9CM) C0478000) =Congenital Abnormality
993. CONG TRICUSP ATRES/STEN
[ ] (UMLS (ICD9CM) C0158616) =Congenital Abnormality ;
944. CONG ANOM OF AORTA NOS
[ ] (UMLS (ICD9CM) C0302467) =Congenital Abnormality
994. CONG VALGUS FOOT DEF NEC
[ ] (UMLS (ICD9CM) C0158728) =Congenital Abnormality
945. Cong anomalies heart/circ syst
[Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS.(MSH)] (UMLS (ICPC) C0243050) (Cong anomalies heart/circ syst; BIOTZEKO ZORTZETIKO ANOMALIA/ZIRKULAZIO SISTEMA; Medfodt misdan i hjerte-kar syst; Aangeboren afw hartvaatstelsel; SYDAMEN/VERENKIERRON SYNNYNNAINEN EPAMUODOSTUMA; Anomalies congen coeur/circul; angeb Missbild des Kreislaufsystems; maxalat lev muledet; sziv/kering. veleszul.rendell.; Anomalie cong cuore/sist circ; MEDFODT FEIL I HJERTE-KAR-SYSTEM; Malf congenita coracao/ap circul; An congenitas corazon/ap circ; MEDFODD MISSBILDNING HJARTA/BLODCIRKULATIONSORGAN) =Congenital Abnormality; Disease or Syndrome =Aangeboren afwijking spijsvert org; ASCVD; CIRCULATORY; Diagnosis/Diseases Component =Arterio-Arterial Fistula; arteriovenous malformation; CONG HEART ANOMALY NOS; Scimitar Syndrome; Atresia of pulmonary valve, congenital; Central Nervous System Vascular Malformation
995. CONG VARUS FOOT DEF NEC
[ ] (UMLS (ICD9CM) C0158725) =Congenital Abnormality
946. CONG AORTA VALV INSUFFIC
[ ] (UMLS (ICD9CM) C0158617) =Congenital Abnormality; Disease or Syndrome
996. CONG/HERID THROMB PURPRA
[ ] (UMLS (ICD9CM) C1561831) Congenital and hereditary thrombocytopenic purpura;
=Disease or Syndrome
947. CONG AORTA VALV STENOSIS
(UMLS (ICD9CM) C0152417) =Congenital Abnormality; Disease or Syndrome
997. CONGEN ABN UTER-ANTEPART
[ ] (UMLS (ICD9CM) C0157009) =Congenital Abnormality; Disease or Syndrome
948. CONG BOWING LEG NOS
(UMLS (ICD9CM) C0152432) =Congenital Abnormality ;
998. CONGEN ABN UTER-POSTPART
[ ] (UMLS (ICD9CM) C0157010) =Disease or Syndrome ;
949. CONG BOWING TIBIA/FIBULA
[ ] (UMLS (ICD9CM) C0158720) =Congenital Abnormality
999. CONGEN ABN UTERUS-DELIV
[ ] (UMLS (ICD9CM) C0157007) =Congenital Abnormality ;
950. CONG CATAR/LENS ANOM NEC
[ ] (UMLS (ICD9CM) C0158554) =Congenital Abnormality ;
1000. CONGEN BOWING OF FEMUR
[ ] (UMLS (ICD9CM) C0158719) =Congenital Abnormality

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