UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ
HYA HYB HYC HYD HYG HYH HYK HYM HYO HYP HYS HYT
selected terms: 494 page 5 of 5

401. Hypoglossal Nerve Neoplasm
(UMLS (NCI) C1263903) Hypoglossal Nerve Neoplasms;
Hypoglossal Nerve Tumor;
Hypoglossal Nerve Tumors;
Neoplasm of Hypoglossal Nerve;
Neoplasm of the Hypoglossal Nerve;
Neoplasm of the Twelfth Cranial Nerve;
Neoplasm of Twelfth Cranial Nerve;
Tumor of Hypoglossal Nerve;
Tumor of the Hypoglossal Nerve;
Tumor of the Twelfth Cranial Nerve;
Tumor of Twelfth Cranial Nerve;
Twelfth Cranial Nerve Neoplasm;
Twelfth Cranial Nerve Neoplasms;
Twelfth Cranial Nerve Tumor;
Twelfth Cranial Nerve Tumors;
XIIth Cranial Nerve Neoplasms;
XIIth Cranial Nerve Tumors;
=Neoplastic Process
448. HYPOSPADIAS
[ ] (UMLS (ICD9CM) C1691215) =Congenital Abnormality
402. Hypoglossal Nerve Neurilemmoma
(UMLS (NCI) C1335928) Hypoglossal Nerve Schwannoma;
Hypoglossal Neurilemmoma;
Hypoglossal Schwannoma;
Neurilemmoma of Hypoglossal Nerve;
Neurilemmoma of the Hypoglossal Nerve;
Neurilemmoma of the Twelfth Cranial Nerve;
Neurilemmoma of Twelfth Cranial Nerve;
Schwannoma of Hypoglossal Nerve;
Schwannoma of the Hypoglossal Nerve;
Schwannoma of the Twelfth Cranial Nerve;
Schwannoma of Twelfth Cranial Nerve;
Twelfth Cranial Nerve Neurilemmoma;
Twelfth Cranial Nerve Schwannoma =Neoplastic Process
449. Hypospadias and epispadias and other penile anomalies
[ ] (UMLS (ICD9CM) C0375526) =Congenital Abnormality
403. Hypoglossal Nucleus
[motor nucleus for the hypoglossal nerve, supplying tongue muscles (all but the palatoglossus). ( CSP )] (UMLS (NCI) C0228802) =Body Part, Organ, or Organ Component =medulla oblongata;
450. HYPOTENSION NEC
[ ] (UMLS (ICD9CM) C0490007) =Disease or Syndrome
404. Hypoglossal-facial anastomosis
[ ] (UMLS (ICD9CM) C0394407) =Therapeutic or Preventive Procedure
451. hypotensive peptide
[ ] (UMLS (CSP) C0598753) =Amino Acid, Peptide, or Protein; Biologically Active Substance
405. Hypoglycemia
[syndrome of abnormally low blood glucose level; clinical hypoglycemia has diverse etiologies; severe hypoglycemia eventually lead to glucose deprivation of the central nervous system resulting in hunger, sweating, paresthesia, impaired mental function, seizures, coma, and even death.(CSP)] (UMLS (ICPC) C0020615) (Hypoglycemia; HIPOGLIZEMIA; Hypoglykaemi; Hypoglykemie; HYPOGLYKEMIA/MATALA VERENSOKERI; Hypoglycemie; Hypoglykaemie; hipoglikemia; hypoglycaemia; Ipoglicemia; LAVT BLODSUKKER/HYPOGLYKEMI; Hipoglicemia; Hipoglucemia; HYPOGLYKEMI) Hypoglycemia =Disease or Syndrome =Metabolic Disease; Endocrine Pancreas Disease; ENDOCRINE, METABOLIC AND NUTRITIONAL; Diagnosis/Diseases Component =hypoglycemia associated with hypoketonemia; Insulin Coma
452. Hypothalamic Hormone
[hormones isolated from the hypothalamus which exercise control over other organs, primarily the pituitary gland; members include certain pituitary hormone-releasing hormones and pituitary hormone release inhibiting hormones. ( CSP )] (UMLS (NCI) C0020656) =Amino Acid, Peptide, or Protein; Hormone =Peptide Hormone;
=ACTH releasing factor;
D-His-6-Pro-8-NEt-LHRH;
neurophysin;
neurotensin;
AY 24910;
GHRH;
PROTIRELIN;
prolactin releasing/inhibiting factor
406. hypoglycemia associated with hypoketonemia
[hypoglycemia that is associated with hypoketonemia, abnormally low glucose and ketones in the blood; patients usually present in the 2nd year of life and hypoglycemia is associated with encephalopathy mimicking Reye's syndrome. ( CSP )] (UMLS (CSP) C0596744) =Disease or Syndrome ;
=Blood Glucose, Low;
453. Hypothalamic Neoplasm
[Benign and malignant tumors of the HYPOTHALAMUS. Pilocytic astrocytomas and hamartomas are relatively frequent histologic types. Neoplasms of the hypothalamus frequently originate from adjacent structures, including the OPTIC CHIASM, optic nerve (see OPTIC NERVE NEOPLASMS), and pituitary gland (see PITUITARY NEOPLASMS). Relatively frequent clinical manifestations include visual loss, developmental delay, macrocephaly, and precocious puberty. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2051) ( MSH )] (UMLS (NCI) C0020659) =Neoplastic Process ;
=Endocrine Gland Neoplasms;
Hypothalamic Diseases;
Brain Neoplasms, Supratentorial;
=Neoplasm of Pituitary;
407. HYPOGLYCEMIC COMA
(UMLS (ICD9CM) C0020617) =Disease or Syndrome
454. hypothalamic pituitary axis
[neuroendocrine system of neurons, fiber tracts, endocrine tissue, and blood vessels which produces and releases pituitary hormones into the systemic circulation. ( CSP )] (UMLS (CSP) C0678897) =Organ or Tissue Function ;
=HPA;
408. hypoglycin
[ ] (UMLS (CSP) C0244602) =Organic Chemical; Hazardous or Poisonous Substance ;
455. hypothalamic pituitary gonadal axis
[ ] (UMLS (CSP) C0814030) =Body Part, Organ, or Organ Component
409. hypoglycorrhachia
[ ] (UMLS (CSP) C0598121) =Laboratory or Test Result
456. hypothalamus
[ventral part of the diencephalon extending from the region of the optic chiasm to the caudal border of the mammillary bodies and forming the inferior and lateral walls of the third ventricle. ( CSP )] (UMLS (NCI) C0020663) =Body Part, Organ, or Organ Component ;
=diencephalon;
=filiform nucleus;
preoptic area;
SCN;
supraoptic nucleus
410. hypogonadism
[condition resulting from or characterized by abnormally decreased functional activity of the gonads, with retardation of growth and sexual development. ( CSP )] (UMLS (CSP) C0020619) =Disease or Syndrome =gonad disorder;
sex development disorder =familial hypogonadism with anosmia;
Hypogonadotropic Hypogonadism;
familial hypogonadism with anosmia;
Eunuchism
457. HYPOTHERMIA
(UMLS (ICD9CM) C0020673) =Therapeutic or Preventive Procedure ;
411. Hypogonadotropic Hypogonadism
[genetic disease that produces sterile males with small testes lacking sperm due to XXY karyotype. ( CSP )] (UMLS (NCI) C0022735) =Congenital Abnormality; Disease or Syndrome =Chromosomal anomalies;
hypogonadism;
Arrieration mentale;
Sex Chromosome Abnormalities;
sex differentiation disorder;
syndrome
458. HYPOTHERMIA
[ ] (UMLS (ICD9CM) C0413252) =Injury or Poisoning
412. hypogonadotropoic eunuchoidism
[ ] (UMLS (CSP) C0598746) =Congenital Abnormality; Disease or Syndrome
459. Hypothermia (systemic) incidental to open heart surgery
(UMLS (ICD9CM) C0189746) =Therapeutic or Preventive Procedure
413. Hypogranular Acute Promyelocytic Leukemia
(UMLS (NCI) C0563634) =Neoplastic Process
460. Hypothesis Test
[A test used to determine the statistical significance of an observation. ( NCI )] (UMLS (NCI) C0237913) =Intellectual Product
414. Hypohidrosis
[Abnormally diminished or absent perspiration. Both generalized and segmented (reduced or absent sweating in circumscribed locations) forms of the disease are usually associated with other underlying conditions. ( MSH )] (UMLS (NCI) C0020620) =Disease or Syndrome =Disorders of sweat glands;
461. Hypothetical Protein FLJ20174
[Encoded by human FLJ20174 Gene, Hypothetical Protein FLJ20174 is a potential homolog of sid-1 (C. elegans), a predicted transmembrane protein localized to the cell periphery, and required cell autonomously for systemic RNA interference (RNAi). (NCI) ( NCI )] (UMLS (NCI) C1334072) SID1;
SID1 Transmembrane Family, Member 1;
SIDT1 =Amino Acid, Peptide, or Protein; Biologically Active Substance
415. hypoimmunity
[deficiency of immune response or a disorder characterized by deficient immune response; classified as antibody (B cell), cellular (T cell), or combined immunodeficiency, or phagocytic dysfunction disorders. ( CSP )] (UMLS (CSP) C0021051) =Disease or Syndrome =immune disorder;
immunopathology =HYPOGAMMAGLOBULINEM NOS;
inborn immunodeficiency;
acquired immunodeficiency;
agammaglobulinemia;
ataxia telangiectasia;
Acquired Agammaglobulinemia;
DiGeorge Anomaly;
Dysgammaglobulinemia;
HIV Infection;
HTLV-BLV Infections;
LYMPHOCYTOPENIA;
Phagocyte Bactericidal Dysfunction;
Aldrich syndrome;
combined T and B cell inborn immunodeficiency;
Leukocyte-Adhesion Deficiency Syndrome;
Immune System Suppression;
462. hypothyroidism
[deficiency of thyroid gland activity; characterized by decreased basal metabolic rate, fatigue and lethargy, sensitivity to cold, and menstrual disturbances; untreated it progresses to myxedema; in infants severe hypothyroidism leads to cretinism. ( CSP )] (UMLS (NCI) C0020676) =Disease or Syndrome ;
=DISORDER OF THYROID NOS;
=Congenital hypothyroidism;
myxedema;
familial hypothyroidism;
Congenital hypothyroidism;
myxedema;
416. hypokalemia
[abnormally low potassium concentration in the blood; may result from excessive potassium loss by the renal or gastrointestinal route, from decreased intake, or from transcellular shifts; manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities, and by renal and gastrointestinal disorders. ( CSP )] (UMLS (CSP) C0020621) =Finding =electrolyte balance;
Water-Electrolyte Imbalance =potassium deficiency;
463. Hypothyroidism/myxedema
(UMLS (ICPC) C0497407) (Hypothyroidism/myxedema; HIPOTIROIDISMOA/MISOEDEMA; Hypotyreose/myksodem; Hypothyreoidie/myxoedeem; KILPIRAUHASEN VAJAATOIMINTA/MYXODEMA; Hypothyroidie/myxoedeme; Hypothyreose/Myxoedem; hipotiroidizm; hypothyreosis/myxoedema; Ipotiroidismo/mixedema; HYPOTYREOSE/MYKSODEM/KRETINISME; Hipotiroidismo/mixedema; Hipotiroidismo/mixedema; HYPOTYREOIDISM/MYXODEM) =Disease or Syndrome =ENDOCRINE, METABOLIC AND NUTRITIONAL; Diagnosis/Diseases Component
417. hypokalemic alkalosis
[ ] (UMLS (CSP) C0085570) =Disease or Syndrome ;
464. Hypotony associated with other ocular disorders
[ ] (UMLS (ICD9CM) C0154784) =Disease or Syndrome ;
418. hypolipemia
[abnormally decreased amount of fat in the blood. ( CSP )] (UMLS (CSP) C0342892) =Pathologic Function =BLOOD DISEASE NOS;
Alteracoes do metabolismo lipidico =hypocholesteremia
465. HYPOTONY DUE TO FISTULA
[ ] (UMLS (ICD9CM) C0154783) =Disease or Syndrome; Anatomical Abnormality
419. hypolipoproteinemia
[presence of abnormally low levels of lipoproteins in the serum. ( CSP )] (UMLS (CSP) C0020623) =Disease or Syndrome =Lipid Metabolism, Inborn Errors;
lipoprotein disorder =familial hypolipoproteinemia;
abetalipoproteinemia;
hypobetalipoproteinemia;
familial cholesteryl ester deficiency;
Tangier disease;
466. HYPOTONY NOS, EYE
[Abnormally low intraocular pressure often related to chronic inflammation (uveitis). ( MSH )] (UMLS (ICD9CM) C0028841) =Disease or Syndrome =Disorder of eye, unspecified;
420. Hypomagnesemia
[Lower than normal levels of magnesium in the circulating blood. ( NCI )] (UMLS (NCI) C0151723) =Finding
467. Hypotrichosis
[Presence of less than the normal amount of hair. (Dorland, 27th ed) ( MSH )] (UMLS (NCI) C0020678) =Disease or Syndrome ;
=Hair Diseases;
=alopecia;
421. hypomania
[ ] (UMLS (CSP) C0241934) =Mental or Behavioral Dysfunction
468. HYPOTRICHOSIS OF EYELID
[ ] (UMLS (ICD9CM) C0155214) =Disease or Syndrome
422. Hypomelanosis of Ito
(UMLS (NCI) C0022283) =Congenital Abnormality; Disease or Syndrome
469. Hypovase
(UMLS (NCI) C0591627) =Organic Chemical; Pharmacologic Substance
423. Hypomelia Hypotrichosis Facial Hemangioma Syndrome
(UMLS (NCI) C0392475) =Congenital Abnormality; Disease or Syndrome ;
470. hypoventilation
[reduction in the amount of air entering the pulmonary alveoli. ( CSP )] (UMLS (CSP) C0398353) =Pathologic Function =Andenod/dyspno;
respiratory insufficiency;
Signs and Symptoms, Respiratory;
=respiratory center dysfunction;
424. Hypomenorrhea
(UMLS (NCI) C0020624) =Disease or Syndrome
471. hypovitaminosis
[condition due to a deficiency of one or more essential vitamins. ( CSP )] (UMLS (CSP) C1510471) Unspecified vitamin deficiency;
vitamin deficiency;
Vitamin Deficiency Disorder;
VITAMIN DEFICIENCY NOS =Disease or Syndrome ;
=dietary deficiency;
=Ascorbic acid deficiency;
Unspecified vitamin A deficiency;
Deficiency of B-complex components;
Unspecified vitamin D deficiency;
vitamin E deficiency;
DEFICIENCY OF VITAMIN K
425. hypomyotonia
[diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching. ( CSP )] (UMLS (CSP) C0026827) =Sign or Symptom =muscle disorder;
neuromuscular manifestation
472. hypovolemia
[abnormally decreased volume of circulating fluid (plasma) in the body. ( CSP )] (UMLS (CSP) C0546884) =Finding =ASCVD;
Metabolic Disease;
Pathologic Process;
426. hyponatremia
[abnormally low sodium levels in the blood; salt depletion. ( CSP )] (UMLS (CSP) C0020625) =Finding =electrolyte balance;
Water-Electrolyte Imbalance
473. hypoxanthine
[6-oxopurine, the base in inosine and its derivatives. ( CSP )] (UMLS (CSP) C0020684) =Organic Chemical; Biologically Active Substance =oxypurine;
427. hypoparathyroidism
[condition produced by greatly reduced function of the parathyroids possibly due to autoimmune disease or genetic factors, or by the removal of those bodies; lack of parathyroid hormone leads to a fall in plasma calcium level, which may result in increase neuromuscular excitability and ultimately tetany followed by a rise in plasma phosphate level. ( CSP )] (UMLS (CSP) C0020626) =Disease or Syndrome =Disorders of parathyroid gland;
=DiGeorge Anomaly;
tetany
474. hypoxanthine guanine phosphoribosyltransferase deficiency
[rare x-linked disorder of purine metabolism, due to deficiency of hypoxanthine phosphoribosyltransferase; affected individuals are normal in the first year of life and then develop psychomotor retardation, extrapyramidal movement disorders, progressive spasticity, and seizures; self-destructive behaviors such as biting of fingers and lips are seen frequently; intellectual impairment may also occur but is typically not severe; elevation of uric acid in the serum leads to the development of renal calculi and gouty arthritis. ( CSP )] (UMLS (CSP) C0023374) =Disease or Syndrome =Arrieration mentale;
purine/pyrimidine metabolism disorder;
syndrome;
enzyme deficiency;
Heredodegenerative Disorders, Nervous System;
Brain Diseases, Metabolic, Inborn
428. Hypopharyngeal Neoplasm
[Tumors or cancer of the HYPOPHARYNX. ( MSH )] (UMLS (NCI) C0020627) =Neoplastic Process =Neoplasm of Pharynx;
475. HYPOXEMIA
(UMLS (ICD9CM) C0700292) =Finding ;
429. Hypopharynx
[The bottom part of the throat. Cancer of the hypopharynx is also called hypopharyngeal cancer. ( NCI )] (UMLS (NCI) C0020629) =Body Location or Region
476. Hypoxemia of newborn
[ ] (UMLS (ICD9CM) C1719628) NB HYPOXIA =Disease or Syndrome
430. hypophosphatasia
[genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia; manifestations include severe skeletal defects resembling vitamin D resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes. ( CSP )] (UMLS (CSP) C0020630) =Disease or Syndrome =Congenital Metabolic Disorder;
inborn metal metabolism disorder;
DIS PHOSPHORUS METABOL;
477. hypoxia
[reduction of oxygen supply to tissue below physiological level. ( CSP )] (UMLS (NCI) C0242184) =Pathologic Function ;
=BLOOD DISEASE NOS;
Pathologic Process;
DISEASES OF THE RESPIRATORY SYSTEM;
Clinical Finding =hypoxia neonatorum
431. hypophosphatemia
[abnormally decreased amounts of phosphates in the blood; manifestations include hemolysis, lassitude, weakness, and convulsions. ( CSP )] (UMLS (CSP) C0085682) =Finding =DIS PHOSPHORUS METABOL;
478. hypoxia neonatorum
[reduction of oxygen supply to tissues in newborns that is below physiological levels. ( CSP )] (UMLS (CSP) C0520599) =Pathologic Function =hypoxia;
432. hypophosphatemia in renal tubular abnormality
[ ] (UMLS (CSP) C0599625) =Disease or Syndrome
479. HYPOXIC-ISCHEMIC ENCEPH
(UMLS (ICD9CM) C0752304) Hypoxic-ischemic encephalopathy (HIE);
=Disease or Syndrome ;
433. hypophosphaturia
[ ] (UMLS (CSP) C0268077) =Disease or Syndrome ;
480. Hysterectomy
(UMLS (HL7) C1548863) =Health Care Activity =Consent Type;
434. hypophysis
[epithelial body located at the base of the brain in the sella turcica, attached by a stalk to the hypothalamus from which it receives important neural and vascular outflow; it consists of the anterior lobe, or adenohypophysis, which secretes most of the hormones, the posterior lobe or neurohypophysis, which stores and releases neurohormones that it receives from the hypothalamus, and an intermediate lobe. ( CSP )] (UMLS (CSP) C0032005) =Body Part, Organ, or Organ Component =Body System, Endocrine/Metabolic;
=neurohypophysis;
481. hysterectomy
[surgical removal of the uterus. ( CSP )] (UMLS (NCI) C0020699) =Therapeutic or Preventive Procedure ;
=reproductive sterilization;
female reproductive system surgery
435. HYPOPIGMENTATION LID
[ ] (UMLS (ICD9CM) C0155212) =Disease or Syndrome
482. HYSTERECTOMY NEC/NOS
[ ] (UMLS (ICD9CM) C0376037) =Therapeutic or Preventive Procedure
436. hypopituitarism
[diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including luteinizing hormone, follicle stimulating hormone, somatotropin; and corticotropin); may result from surgical or radiation ablation, non-secretory pituitary neoplasms, metastatic tumors, infarction, pituitary apoplexy, infiltrative or granulomatous processes, and other conditions. ( CSP )] (UMLS (CSP) C0020635) =Disease or Syndrome =Pituitary Diseases;
=diabetes insipidus;
Dwarfism, Pituitary;
diabetes insipidus;
Dwarfism, Pituitary
483. Hysterectomy, Vaginal
[A surgical procedure to remove the uterine body and cervix, via the vaginal approach. ( NCI )] (UMLS (NCI) C0020700) =Therapeutic or Preventive Procedure ;
437. HYPOPLAS LEFT HEART SYND
[A condition caused by underdevelopment of the whole left half of the heart. It is characterized by hypoplasia of the left cardiac chambers (ATRIUM; VENTRICLE), the AORTA, the AORTIC VALVE, and the MITRAL VALVE. Severe symptoms appear in early infancy when DUCTUS ARTERIOSUS closes. ( MSH )] (UMLS (ICD9CM) C0152101) =Congenital Abnormality; Disease or Syndrome =CONG HEART ANOMALY NOS;
484. hysteria
[behavior exhibiting excessive or uncontrollable emotion, such as fear or panic; mental disorder characterized by emotional excitability and sometimes by amnesia or a physical deficit, such as paralysis, or a sensory deficit, without an organic cause. ( CSP )] (UMLS (CSP) C0020701) =Mental or Behavioral Dysfunction =HISTRIONIC PERSON NOS;
Neurotic Disorders =catalepsy;
DISSOCIATIVE FUGUE
438. Hypoplasia of Vagina
(UMLS (NCI) C0345309) =Congenital Abnormality ;
485. hysterical neurosis
[ ] (UMLS (CSP) C0086441) =Mental or Behavioral Dysfunction
439. hypoplastic anemia
[ ] (UMLS (CSP) C0178416) =Disease or Syndrome ;
486. Hysterical/hypochondriacal disease
(UMLS (ICPC) C0497331) (Hysterical/hypochondriacal disease; HISTERIA/HIPOKONDRIASIA; Hysteriform/hypokondrisk tilstand; Hysterie/hypochondrie; HYSTEERINEN/HYPOKONDRINEN OIRE; Trouble hysterique/hypochondr; Hysterie/Hypochondrie/Somatisierung; histeria o hipoxondria; hiszteria/hipochondria; Disturbo isterico/ipocondriaco; HYSTERIFORM/HYPOKONDRISK TILSTAND; Alt histericas/hipocondriacas; Alt histericas/hipocondriacas; HYSTERISK/HYPOKONDRISK STORNING) Hysterical/hypochondriacal dis =Mental or Behavioral Dysfunction =Diagnosis/Diseases Component; PSYCHOLOGICAL
440. Hypopomus
[ ] (UMLS (CSP) C0599052) =Fish
487. hysterogram
[ ] (UMLS (CSP) C0203039) =Diagnostic Procedure
441. hypoproteinemia
[condition in which total serum protein level is below the normal range; can be caused by protein malabsorption in the gastrointestinal tract, edema, or proteinuria. ( CSP )] (UMLS (CSP) C0020639) =Sign or Symptom =blood protein disorder;
protein metabolism disorder =hypoalbuminemia;
488. Hysterosalpingogram
(UMLS (HL7) C1548864) =Health Care Activity =Consent Type;
442. HYPOPYON
[An accumulation of pus in the anterior chamber of the eye. ( NCI )] (UMLS (ICD9CM) C0020641) =Disease or Syndrome
489. HYSTEROSCOPY
[Endoscopic examination, therapy or surgery of the interior of the uterus. ( MSH )] (UMLS (ICD9CM) C0020710) =Diagnostic Procedure
443. HYPOPYON ULCER
[ ] (UMLS (ICD9CM) C0155070) =Disease or Syndrome ;
490. HYSTEROTOMY
[An incision in the uterus, performed through either the abdomen or the vagina. ( MSH )] (UMLS (ICD9CM) C0020711) =Therapeutic or Preventive Procedure
444. hyporeninemic hypoaldosteronism
[selective aldosterone deficiency resulting from low renin production. ( CSP )] (UMLS (CSP) C0376185) =Disease or Syndrome ;
=Hypoaldosteronism;
491. HYSTEROTOMY TO TERMIN PG
[ ] (UMLS (ICD9CM) C0195643) =Therapeutic or Preventive Procedure
445. hyposmia
[ ] (UMLS (CSP) C0234260) =Finding
492. Hytrin
(UMLS (NCI) C0591628) =Organic Chemical; Pharmacologic Substance
446. HYPOSMOLALITY
(UMLS (ICD9CM) C0020645) =Disease or Syndrome
493. [1-Hydroxy-2-(1H-imidazol-1-yl)ethylidene]bisphosphonic Acid
[The brand name for zoledronic acid, a bisphosphonic imidazol compound which inhibits osteoclastic bone resorption. Although its mechanisms of action is yet to be fully characterized, zoledronic acid appears to directly inhibit osteoclast function and trigger osteoclast apoptotic cell death, thereby decreasing the osteoclast stimulation and bone calcium loss induced by various tumor-associated cytokines. Check for "http://www.cancer.gov/Search/ClinicalTrialsLink.aspx?id=42507&idtype=1" active clinical trials or "http://www.cancer.gov/Search/ClinicalTrialsLink.aspx?id=42507&idtype=1&closed=1" closed clinical trials using this agent. ("http://nciterms.nci.nih.gov:80/NCIBrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&code=C1699" NCI Thesaurus) ( PDQ )] (UMLS (NCI) C0392938) =Organophosphorus Compound; Pharmacologic Substance
447. Hypospadia
[A birth defect due to malformation of the URETHRA in which the urethral opening is below its normal location. In the male, the malformed urethra generally opens on the ventral surface of the PENIS or on the PERINEUM. In the female, the malformed urethral opening is in the VAGINA.(MSH)] (UMLS (ICPC) C0848558) (Hypospadia; (194); Hyspospadi; Hypospadie; SIITTIMEN ALAHALKIO; Hypospadias; Hypospadie; (108); hypospadiasis; Ipospadia; HYPOSPADI q54; Hipospadias; Hipospadias; HYPOSPADI) HYPOSPADI; HYPOSPADI q54; Hypospadia; Hypospadias; hypospadiasis; Hypospadie; Hyspospadi; Ipospadia; SIITTIMEN ALAHALKIO =Congenital Abnormality =DISORDER OF PENIS NOS; Congenital Genitourinary Abnormality; Diagnosis/Diseases Component; Body System, Reproductive, Male
494. [6-Hydroxy-2-(4-hydroxyphenyl)-benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone
[a selective estrogen receptor modulator; has both agonist and antagonist estrogen action. ( CSP )] (UMLS (NCI) C0244404) =Organic Chemical; Pharmacologic Substance ;
=Antiestrogen;
estrogen analog;
1-p-beta-dimethylamino-ethoxyphenyl-trans-1,2-diphenylbut-1-ene;
selective estrogen receptor modulator;
[HS900] HORMONES/SYNTHETICS/MODIFIERS, OTHER;
=6-Hydroxy-2-(4-hydroxyphenyl)benzo(b)thien-3-yl)(4-(2-(1-piperidinyl)ethoxy)phenyl)methanone Hydrochloride

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