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 3 of 5

201. Hypaque
(UMLS (NCI) C0813724) =Organic Chemical; Indicator, Reagent, or Diagnostic Aid ;
251. HYPERKINETIC HEART DIS
(UMLS (ICD9CM) C0242407) =Disease or Syndrome ;
202. HYPERACT LABYRINTH BILAT
[ ] (UMLS (ICD9CM) C0155516) =Disease or Syndrome
252. hyperlipemia
[excess of lipids in the blood. ( CSP )] (UMLS (CSP) C0020473) =Disease or Syndrome =BLOOD DISEASE NOS;
Metabolic Disease;
Alteracoes do metabolismo lipidico;
=hypercholesteremia;
hypertriglyceridemia;
hypercholesteremia;
hyperlipoproteinemia;
hypertriglyceridemia;
203. hyperactive child
[ ] (UMLS (CSP) C1691214) =Mental or Behavioral Dysfunction
253. HYPERLIPIDEMIA NEC/NOS
[ ] (UMLS (ICD9CM) C0348494) =Disease or Syndrome
204. Hyperactive labyrinth, unilateral
[ ] (UMLS (ICD9CM) C0155515) =Disease or Syndrome
254. hyperlipoproteinemia
[metabolic disease characterized by excess plasma lipoproteins, due to a disorder of lipoprotein metabolism; may be acquired or familial. ( CSP )] (UMLS (CSP) C0020476) =Disease or Syndrome =hyperlipemia;
Lipid Metabolism, Inborn Errors;
lipoprotein disorder;
=familial hyperlipoproteinemia;
Hyperlipidemia, Familial Combined;
broad beta disease;
familial hyperlipoproteinemia type V;
Burger Grutz syndrome;
205. Hyperactivity
[Excessive movement of muscles of the body as a whole, which may be associated with organic or psychological disorders. ( MSH )] (UMLS (NCI) C0424295) =Finding =Dyscinesia;
255. hyperlysinemia
[A group of inherited metabolic disorders which have in common elevations of serum LYSINE levels. Enzyme deficiencies of alpha-aminoadipic semialdehyde dehydrogenase and the SACCHAROPINE DEHYDROGENASES have been associated with hyperlysinemia. Clinical manifestations include mental retardation, recurrent emesis, hypotonia, lethargy, diarrhea, and developmental delay. (From Menkes, Textbook of Child Neurology, 5th ed, p56) ( MSH )] (UMLS (CSP) C0268553) =Disease or Syndrome =Amino Acid Metabolism, Inborn Errors;
206. HYPERACUSIS
[An abnormally disproportionate increase in the sensation of loudness in response to auditory stimuli of normal volume. COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; FACIAL NERVE DISEASES; STAPES SURGERY; and other disorders may be associated with this condition. ( MSH )] (UMLS (ICD9CM) C0034880) =Sign or Symptom =hearing disorder;
256. HYPERMATURE CATARACT
(UMLS (ICD9CM) C0152258) =Disease or Syndrome ;
207. hyperalgesia
[excessive sensitivity to painful stimuli. ( CSP )] (UMLS (CSP) C0020429) =Finding =pain;
Somatosensory Disorders
257. Hypermedia
[A computer environment in which multiple linkages enable users to move directly from one segment of audio, video, graphic, or text to another in a database. ( NCI )] (UMLS (NCI) C0376429) =Intellectual Product ;
208. hyperalimentation therapy
[Total parenteral nutrition formulated for intravenous administration in patients who cannot eat or cannot get enough nutrients from the foods they eat. It is a liquid mixture of proteins, carbohydrates, fats, vitamins, minerals and other nutrients. ( NCI )] (UMLS (CSP) C0030548) =Therapeutic or Preventive Procedure ;
258. HYPERMETROPIA
[A refractive error in which rays of light entering the eye parallel to the optic axis are brought to a focus behind the retina, as a result of the eyeball being too short from front to back. It is also called farsightedness because the near point is more distant than it is in emmetropia with an equal amplitude of accommodation. (Dorland, 27th ed) ( MSH )] (UMLS (ICD9CM) C0020490) =Disease or Syndrome =Alteraciones de la refraccion;
209. hyperandrogenism
[A condition caused by the excessive secretion of ANDROGENS from the ADRENAL CORTEX; the OVARIES; or the TESTES. The clinical significance in males is negligible. In women, the common manifestations are HIRSUTISM and VIRILISM as seen in patients with POLYCYSTIC OVARY SYNDROME and ADRENOCORTICAL HYPERFUNCTION. ( MSH )] (UMLS (CSP) C0206081) =Disease or Syndrome =gonad disorder;
259. HYPERMOBILITY OF COCCYX
[ ] (UMLS (ICD9CM) C0158295) =Disease or Syndrome ;
210. hyperbaric chamber
[compartment in which air pressure may be raised to greater than atmospheric pressure. ( CSP )] (UMLS (CSP) C0175726) =Medical Device ;
=controlled environment chamber;
260. HYPERMOBILITY SYNDROME
[ ] (UMLS (ICD9CM) C0152093) =Disease or Syndrome
211. Hyperbaric Oxygen
[Oxygen that is at an atmospheric pressure higher than the pressure at sea level. Breathing hyperbaric oxygen to enhance the effectiveness of radiation therapy is being studied. ( NCI )] (UMLS (NCI) C0279328) =Pharmacologic Substance
261. hypermyotonia
[abnormal increase in skeletal or smooth muscle tone; skeletal muscle hypertonicity may be associated with pyramidal tract lesions or basal ganglia diseases. ( CSP )] (UMLS (CSP) C0026826) =Sign or Symptom =muscle disorder;
neuromuscular manifestation =muscle rigidity;
Muscle Spasticity
212. hyperbaric oxygen therapy
[therapeutic intermittent administration of oxygen in a chamber at greater than sea-level atmospheric pressures; considered effective treatment for air and gas embolisims, smoke inhalation, acute carbon monoxide poisoning, caisson disease, clostridial gangrene, etc. ( CSP )] (UMLS (CSP) C0020431) =Therapeutic or Preventive Procedure =oxygen administration;
262. hypernatremia
[excessive amount of sodium in the blood. ( CSP )] (UMLS (CSP) C0020488) =Disease or Syndrome =electrolyte balance;
Water-Electrolyte Imbalance
213. hyperbaric sickness
[Progressive mental disturbances and unconsciousness due to breathing mixtures of oxygen and inert gases (argon, helium, xenon, krypton, and atmospheric nitrogen) at high pressure. ( MSH )] (UMLS (CSP) C0021268) =Injury or Poisoning =gas poisoning;
occupational disease
263. hyperornithinemia
[excess of ornithine in the plasma, such as occurs in the genetic disorders gyrate atrophy of choroid and retina and hyperornithinemia-hyperamonemia-homocitrullinuria syndrome. ( CSP )] (UMLS (CSP) C0599035) =Disease or Syndrome ;
=Amino Acid Metabolism, Inborn Errors;
Degeneration of retina;
enzyme deficiency;
214. hyperbilirubinemia
[pathologic process consisting of an abnormal increase in the amount of bilirubin in the circulating blood, which may result in jaundice. ( CSP )] (UMLS (CSP) C0020433) =Disease or Syndrome =Metabolic Disease;
Pathologic Process =hereditary hyperbilirubinemia;
bilirubin encephalopathy;
neonatal transient jaundice;
Geelzucht;
bilirubin encephalopathy;
264. HYPEROSMOLALITY
[ ] (UMLS (ICD9CM) C0342580) =Disease or Syndrome
215. hypercalcemia
[abnormally high level of calcium in the blood; manifestations include fatigability, muscle weakness, depression, anorexia, nausea, and constipation. ( CSP )] (UMLS (NCI) C0020437) =Disease or Syndrome =calcium metabolism disorder;
Water-Electrolyte Imbalance;
calcium disorder;
265. HYPEROSTOSIS OF SKULL
(UMLS (ICD9CM) C0020496) =Anatomical Abnormality
216. Hypercalcemia of Malignancy
[Hypercalcemia generally develops as a late complication of malignancy; its appearance has grave prognostic significance. It remains unclear, however, whether death is associated with hypercalcemic crisis (uncontrolled or recurrent progressive hypercalcemia) or with advanced disease. Symptoms include central nervous system impairment such as as delirium with prominent symptoms of personality change, cognitive dysfunction, disorientation, incoherent speech, and psychotic symptoms such as hallucinations and delusions, smooth muscle hypotonicity, and altered cardiovascular function. ( NCI )] (UMLS (NCI) C0149911) =Disease or Syndrome
266. hyperoxia
[abnormal increase in the amount of oxygen in the tissues and organs. ( CSP )] (UMLS (CSP) C0242706) =Sign or Symptom ;
=gas poisoning;
Signs and Symptoms, Respiratory
217. Hypercalcemic Sarcoidosis
(UMLS (NCI) C1334067) =Disease or Syndrome ;
267. hyperparathyroidism
[abnormally increased activity of the parathyroid glands, which may be primary or secondary; primary hyperparathyroidism is associated with neoplasia or hyperplasia; excess of parathyroid hormone leads to alteration in function of bone, renal tubules, and gastrointestinal mucosa. ( CSP )] (UMLS (CSP) C0020502) =Disease or Syndrome =Disorders of parathyroid gland;
=Hyperparathyroidism, Secondary
218. hypercalcinuria
[abnormally high calcium in the urine; may be due to hyperabsorption of calcium, with the formation of calcium oxalate or calcium phosphate renal stones. ( CSP )] (UMLS (CSP) C0020438) =Disease or Syndrome =calcium disorder;
268. HYPERPARATHYROIDISM NEC
[ ] (UMLS (ICD9CM) C0348455) =Disease or Syndrome
219. Hypercellular Bone Marrow
(UMLS (NCI) C1334068) =Finding ;
269. hyperphagia
[ingestion of a greater than optimal quantity of food. ( CSP )] (UMLS (CSP) C0020505) =Mental or Behavioral Dysfunction =eating;
Eating Disorders;
gastrointestinal sign/symptom;
220. HYPERCEMENTOSIS
[A regressive change of teeth characterized by excessive development of secondary cementum on the tooth surface. It may occur on any part of the root, but the apical two-thirds are most commonly affected. (Dorland, 27th ed) ( MSH )] (UMLS (ICD9CM) C0020441) =Disease or Syndrome =Dental Disorder;
270. hyperphenylalaninemia
[any of several autosomal recessive defects in the hydroxylation of phenylalanine resulting in accumulation and excretion of dietary phenylalanine; most commonly the defect is in the enzyme phenylalanine 4-monooxygenase; the most severe manifestation of this is classic PHENYLKETONURIA, but two benign forms also occur; rarely the defect is one of tetrahydrobiopterin metabolism. ( CSP )] (UMLS (CSP) C0751435) =Disease or Syndrome =Amino Acid Metabolism, Inborn Errors;
221. hypercholesteremia
[abnormally high levels of cholesterol in the blood. ( CSP )] (UMLS (CSP) C0020443) =Disease or Syndrome =hyperlipemia;
=familial hyperbetalipoproteinemia;
271. HYPERPIGMENTATION LID
[ ] (UMLS (ICD9CM) C0155211) =Disease or Syndrome
222. hypercortisolemia
[ ] (UMLS (CSP) C0598639) =Disease or Syndrome ;
272. hyperpituitarism
[diminution or cessatin of anterior pituitary function; leads to a variety of hormone deficiencies. ( CSP )] (UMLS (CSP) C0020506) =Disease or Syndrome =Pituitary Diseases;
=acromegaly;
gigantism;
acromegaly;
gigantism;
hyperprolactinemia
223. hypercupremia
[ ] (UMLS (CSP) C0268072) =Disease or Syndrome
273. hyperplasia
[abnormal multiplication of otherwise normal cells, leading to tissue enlargement. ( CSP )] (UMLS (NCI) C0020507) =Pathologic Function =Pathologic Process;
Clinical Finding =kidney hyperplasia;
Hyperplasia of Parathyroid;
connective tissue hyperplasia;
oral pharyngeal hyperplasia;
pancreatic islet hyperplasia;
skin hyperplasia;
Adrenal Gland Hyperplasia;
Benign Hyperplasia of Prostate;
224. HYPEREM W METAB DIS-DEL
[ ] (UMLS (ICD9CM) C0156697) =Disease or Syndrome
274. HYPERPLASIA OF APPENDIX
(UMLS (ICD9CM) C1384587) Hyperplasia of appendix (lymphoid) =Pathologic Function ;
225. HYPEREM W METAB DIS-UNSP
[ ] (UMLS (ICD9CM) C0156696) =Disease or Syndrome
275. Hyperplasia of Parathyroid
[abnormal increase in the number of otherwise normal cells in the parathyroid gland without tumor formation that leading to enlargement of the gland; it differs from hypertrophy, which is an increase in bulk without an increase in the number of cells. ( CSP )] (UMLS (NCI) C0271844) =Disease or Syndrome =hyperplasia;
Disorders of parathyroid gland
226. HYPEREM W METAB-ANTEPART
[ ] (UMLS (ICD9CM) C0156698) =Disease or Syndrome
276. Hyperplasia of prostate
[Increase in constituent cells in the PROSTATE, leading to enlargement of the organ (hypertrophy) and adverse impact on the lower urinary tract function. This can be caused by increased rate of cell proliferation, reduced rate of cell death, or both. ( MSH )] (UMLS (ICD9CM) C1739363) Hyperplasia of prostate, unspecified;
prostate hyperplasia;
Prostatic Hyperplasia =Pathologic Function ;
=Prostate Disease;
227. Hyperemesis gravidarum with metabolic disturbance
(UMLS (ICD9CM) C0405080) =Disease or Syndrome ;
277. Hyperplasia of renal artery
[ ] (UMLS (ICD9CM) C0155761) =Acquired Abnormality; Disease or Syndrome
228. HYPEREMIA OF CONJUNCTIVA
(UMLS (ICD9CM) C1761613) =Finding
278. Hyperplastic Polyp
[A polyp found mainly in the stomach and colon. Microscopically, it is characterized by elongated, serrated crypts lined by proliferative epithelium. Hyperplastic polyps are traditionally considered non-neoplastic, but ras mutation is common, clonality has been demonstrated and biochemical abnormalities and epidemiological associations that occur in colorectal adenomas and carcinomas have been found (WHO Tumors of the Digestive System, 2000). However, a number of Gastrointestinal Pathologists reject the idea that hyperplastic polyps represent true neoplasms. —2002 ( NCI )] (UMLS (NCI) C0333983) =Neoplastic Process
229. HYPERESTROGENISM
[ ] (UMLS (ICD9CM) C0154209) =Disease or Syndrome
279. Hyperplastic Polyp of Rectum
(UMLS (NCI) C1335679) Hyperplastic Polyp of the Rectum;
Rectal Hyperplastic Polyp =Disease or Syndrome ;
230. Hypergammaglobulinemia
[An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. ( MSH )] (UMLS (NCI) C0020455) =Disease or Syndrome =blood protein disorder;
Immunoproliferative Disorders =Benign Monoclonal Gammopathy;
280. hyperpnea
[abnormal increase in the depth and rate of respiratory movements. ( CSP )] (UMLS (CSP) C0220854) =Pathologic Function =DISEASES OF THE RESPIRATORY SYSTEM;
231. hyperglobulinemia
[abnormally high globulin content of the blood. ( CSP )] (UMLS (CSP) C1306857) =Finding ;
=hyperproteinemia;
281. hyperprolactinemia
[increased levels of prolactin in the blood, which may be associated with amenorrhea and galactorrhea; relatively common etiologies include prolactinoma, medication effect, kidney failure, granulomatous diseases of the pituitary gland, and disorders which interfere with the hypothalamic inhibition of prolactin release; ectopic (non-pituitary) production of prolactin may also occur. ( CSP )] (UMLS (CSP) C0020514) =Disease or Syndrome =hyperpituitarism;
Metabolic Disease;
Pituitary Diseases;
232. hyperglucagonemia
[abnormally high levels of glucagon in the blood. ( CSP )] (UMLS (CSP) C0342218) =Pathologic Function ;
=Endocrine Pancreas Disease;
282. hyperproteinemia
[presence of an abnormally high amount of protein in the blood. ( CSP )] (UMLS (CSP) C0267988) =Disease or Syndrome =blood protein disorder;
protein metabolism disorder =hyperglobulinemia;
233. hyperglycemic agent
[biologically active substance that causes an increase in the level of glucose in the blood. ( CSP )] (UMLS (CSP) C1321567) =Pharmacologic Substance ;
=Drug;
283. Hyperreflexia
(UMLS (NCI) C0151889) =Finding
234. Hypergranular Acute Promyelocytic Leukemia
(UMLS (NCI) C1336843) Typical Acute Promyelocytic Leukemia =Neoplastic Process ;
284. HYPERSECRETION GLAUCOMA
[ ] (UMLS (ICD9CM) C0154968) =Disease or Syndrome ;
235. hyperhidrosis
[Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise. ( MSH )] (UMLS (CSP) C0020458) =Finding =Disorders of sweat glands;
=Sweating, Gustatory;
285. HYPERSENSIT ANGIITIS NEC
[ ] (UMLS (ICD9CM) C0155758) =Disease or Syndrome ;
236. hyperhomocysteinemia
[An inborn error of methionone metabolism which produces an excess of homocysteine in the blood. It is often caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and is a risk factor for coronary vascular disease. ( MSH )] (UMLS (CSP) C0598608) =Disease or Syndrome =Amino Acid Metabolism, Inborn Errors;
286. HYPERSENSIT ANGIITIS NOS
[Heterogeneous group of disorders characterized by a vasculitic syndrome presumed to be associated with a hypersensitivity reaction following exposure to an antigen such as an infectious agent, a drug, or other foreign or endogenous substance (Wilson et al, Harrison's Principles of Internal Medicine, 12th ed, p1459). ( MSH )] (UMLS (ICD9CM) C0151436) =Disease or Syndrome ;
=immune complex disease;
angiitis =ALLERGIC PURPURA;
Allergic Cutaneous Angiitis;
237. Hypericin
[An anthraquinone derivative that is naturally found in the yellow flower of Hypericum perforatum, St John's wort, with antidepressant, potential antiviral, antineoplastic and immunostimulating activities. Hypericin appears to inhibit the neuronal uptake of serotonin, norepinephrine, dopamine, gamma-amino butyric acid (GABA) and L-glutamate, which may contribute to its antidepressant effect. Hypericin may also prevent the replication of encapsulated viruses probably due to inhibition of the assembly and shedding of virus particles in infected cells. This agent also exerts potent phototoxic effects by triggering apoptotic signaling that results in formation of reactive oxygen species. ( NCI )] (UMLS (NCI) C0063220) =Organic Chemical; Pharmacologic Substance
287. hypersensitivity test
[epicutaneous or intradermal application of a sensitizer for demonstration of either delayed or immediate hypersensitivity; used in diagnosis of hypersensitivity or as a test for cellular immunity. ( CSP )] (UMLS (CSP) C0037296) =Diagnostic Procedure =immunologic assay;
=ppd (purified protein derivative of tuberculin);
238. hypericum
[Genus of perennial plants in the family CLUSIACEAE (sometimes classified as Hypericaceae). Herbal and homeopathic preparations are used for depression, neuralgias, and a variety of other conditions. Hypericum contains flavonoids; GLYCOSIDES; mucilage, TANNINS; volatile oils (OILS, ESSENTIAL), hypericin and hyperforin. ( MSH )] (UMLS (CSP) C1256259) =Plant ;
288. HYPERSOM DT MENTAL DISOR
[ ] (UMLS (ICD9CM) C1561858) Hypersomnia due to mental disorder;
=Mental or Behavioral Dysfunction
239. hypericum perforatum
[St. John's wort. An herbal product sold as an over-the-counter treatment for depression. It is being studied for its ability to lessen certain side effects of cancer treatment. ( NCI )] (UMLS (NCI) C0813171) Hypericum Perforatum Extract;
HYPERICUM PERFORATUM PREPARATION;
St John's Wort;
St. John's Wort;
ST. JOHN'S WORT EXTRACT =Organic Chemical; Pharmacologic Substance ;
=Unclassified Ingredients;
Unclassified Ingredient Preparations =ST. JOHN'S WORT CAP/TAB
289. HYPERSOM W SLP APNEA NOS
[ ] (UMLS (ICD9CM) C1561815) Hypersomnia with sleep apnea, unspecified;
=Sign or Symptom
240. hyperimmunization
[immunization designed to stimulate the production of very large quantities of antibody by the repeated administration of antigen. ( CSP )] (UMLS (CSP) C0596742) =Therapeutic or Preventive Procedure ;
=immunization;
290. Hypersomnia due to medical condition classified elsewhere
[ ] (UMLS (ICD9CM) C1561857) HYPERSOMNIA IN OTHER DIS;
=Disease or Syndrome
241. Hyperimmunoglobulin E Syndrome
[A disorder of neutrophils characterized by the presence of abnormal or absent chemotactic responses and hyperimmunoglobulinemia E. It is transmitted as an autosomal recessive trait and most cases reported have been in girls. ( MSH )] (UMLS (NCI) C0022398) =Disease or Syndrome ;
=Phagocyte Bactericidal Dysfunction;
291. HYPERSOMNIA NOS
(UMLS (ICD9CM) C0917799) Hypersomnia, unspecified;
=Sign or Symptom
242. Hyperimmunoglobulin M Syndrome
[An immunodeficiency state characterized by very low serum IgG and IgA but either a normal or, more frequently, a markedly elevated concentration of polyclonal IgM. ( NCI )] (UMLS (NCI) C0272236) =Disease or Syndrome
292. HYPERSPLENISM
[Condition characterized by splenomegaly, some reduction in the number of circulating blood cells in the presence of a normal or hyperactive bone marrow, and the potential for reversal by splenectomy. ( MSH )] (UMLS (ICD9CM) C0020532) =Disease or Syndrome =Disease of spleen, unspecified;
243. Hyperimmunoglobulin Syndrome
(UMLS (NCI) C1334069) =Disease or Syndrome ;
293. Hypertelorism
[Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid. ( MSH )] (UMLS (NCI) C0020534) =Congenital Abnormality =craniofacial dysostosis;
244. hyperinsulinemia
[syndrome with excessively high insulin levels in the blood; it may cause hypoglycemia; etiology of hyperinsulinism varies, including hypersecretion of a beta cell tumor, autoantibodies against insulin, defective insulin receptor, or overuse of exogeneous insulin or hypoglycemic agents. ( CSP )] (UMLS (CSP) C0020459) =Disease or Syndrome =Endocrine Disease;
Metabolic Disease;
Endocrine Pancreas Disease;
=metabolic syndrome;
294. HYPERTEN PREG NOS-UNSPEC
[ ] (UMLS (ICD9CM) C0156686) =Disease or Syndrome
245. Hyperkalemia
[abnormally high potassium concentration in the blood, most often due to defective renal excretion; characterized clinically by electrocardiographic abnormalities; in severe cases, weakness and flaccid paralysis may occur. ( CSP )] (UMLS (NCI) C0020461) =Finding =electrolyte balance;
Water-Electrolyte Imbalance
295. HYPERTENS ENCEPHALOPATHY
[Brain dysfunction or damage resulting from sustained MALIGNANT HYPERTENSION. When BLOOD PRESSURE exceeds the limits of cerebral autoregulation, cerebral blood flow is impaired (BRAIN ISCHEMIA). Clinical manifestations include HEADACHE; NAUSEA; VOMITING; SEIZURES; altered mental status (in some cases progressing to COMA); PAPILLEDEMA; and RETINAL HEMORRHAGE. ( MSH )] (UMLS (ICD9CM) C0151620) =Disease or Syndrome =Hypertension, Malignant;
Intracranial Hypertension
246. Hyperkeratosis
(UMLS (NCI) C0870082) =Disease or Syndrome ;
296. HYPERTENS NOS-ANTEPARTUM
[ ] (UMLS (ICD9CM) C0156689) =Disease or Syndrome
247. Hyperkeratosis due to yaws
(UMLS (ICD9CM) C0276001) =Disease or Syndrome
297. HYPERTENS NOS-DEL W P/P
[ ] (UMLS (ICD9CM) C0156688) =Disease or Syndrome
248. Hyperkinesis of childhood with developmental delay
[ ] (UMLS (ICD9CM) C0154627) =Mental or Behavioral Dysfunction
298. HYPERTENS NOS-DELIVERED
[ ] (UMLS (ICD9CM) C0156687) =Disease or Syndrome
249. hyperkinetic child
[ ] (UMLS (CSP) C0597927) =Patient or Disabled Group ;
299. HYPERTENS NOS-POSTPARTUM
[ ] (UMLS (ICD9CM) C0156690) =Disease or Syndrome
250. HYPERKINETIC CONDUCT DIS
[ ] (UMLS (ICD9CM) C0154628) =Mental or Behavioral Dysfunction
300. Hypertension Associated Disorders of Pregnancy
(UMLS (NCI) C0852260) Hypertension-Associated Pregnancy Disorder =Pathologic Function ;

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