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
F F F- F0 FA FB FC FD FE FF FG FH FI FJ FK FL FM FN FO FP FR FS FT FU FX FY
FA FAA FAB FAC FAD FAE FAI FAK FAL FAM FAN FAP FAR FAS FAT FAU FAV FAX
selected terms: 443 page 3 of 5

201. FALLOPIAN TUBE OP NEC
[ ] (UMLS (ICD9CM) C0175610) =Therapeutic or Preventive Procedure
251. familial hyperlipoproteinemia type V
[A severe type of hyperlipidemia, sometimes familial, that it is characterized by the elevation of both plasma CHYLOMICRONS and TRIGLYCERIDES contained in VERY-LOW-DENSITY LIPOPROTEINS. Type V hyperlipoproteinemia is often associated with DIABETES MELLITUS and is not caused by reduced LIPOPROTEIN LIPASE activity as in HYPERLIPOPROTEINEMIA TYPE I . ( MSH )] (UMLS (CSP) C0020481) =Disease or Syndrome =hyperlipoproteinemia;
202. Fallopian Tube Papillary Adenocarcinoma
(UMLS (NCI) C1333595) Papillary Adenocarcinoma of Fallopian Tube;
Papillary Adenocarcinoma of the Fallopian Tube =Neoplastic Process
252. familial hypogonadism with anosmia
[anosmia due to failure of the olfactory lobes to develop, with secondary hypogonadism due to gonadotropic hormone deficiency. ( CSP )] (UMLS (CSP) C0162809) =Disease or Syndrome ;
=anosmia;
hypogonadism;
Sex Chromosome Abnormalities;
sex differentiation disorder;
syndrome;
congenital disorder
203. Fallopian Tube Squamous Cell Carcinoma
(UMLS (NCI) C1333596) Squamous Cell Carcinoma of Fallopian Tube;
Squamous Cell Carcinoma of the Fallopian Tube =Neoplastic Process
253. familial hypolipoproteinemia
[inherited diseases characterized by the presence of abnormally low levels of lipoproteins in the blood. ( CSP )] (UMLS (CSP) C0268197) =Disease or Syndrome ;
=hypolipoproteinemia;
inborn lipid/lipoprotein disorder =abetalipoproteinemia;
familial cholesteryl ester deficiency;
Tangier disease;
204. fallopian tube surgery
[procedures performed on the fallopian tubes, used in the treatment of disease, injuries, or deformities; includes excision of all or portions of the fallopian tubes. ( CSP )] (UMLS (CSP) C0195463) =Therapeutic or Preventive Procedure =reproductive sterilization;
female reproductive system surgery
254. familial hypophosphatemia in rickets
[group of disorders characterized by rickets but not responding to high doses of vitamin D; most are forms of familial hypophosphatemic rickets. ( CSP )] (UMLS (CSP) C0733682) hypophosphatemia in rickets;
vitamin D resistant rickets;
X linked hypophosphatemia in rickets =Disease or Syndrome =DIS PHOSPHORUS METABOL;
rickets;
inborn biological transport disorder;
205. False Alarm
[A test result that shows evidence of a result or condition although it is not actually present. ( NCI )] (UMLS (NCI) C0205557) =Finding
255. familial hypothyroidism
[inherited deficiency of thyroid gland activity. ( CSP )] (UMLS (CSP) C0596558) =Disease or Syndrome =Genetic Condition;
hypothyroidism
206. FALSE POS SERO TEST-SYPH
[ ] (UMLS (ICD9CM) C0159128) =Finding
256. Familial Meningioma
(UMLS (NCI) C1333989) Hereditary Meningioma =Neoplastic Process ;
207. false pregnancy
[absence of menses accompanied by other signs of pregnancy without conception; may be due to psychogenic factors, abdominal neoplasia, or a hormonal disorder. ( CSP )] (UMLS (CSP) C0033831) =Pathologic Function =FEMALE GENITAL DIS NOS;
Female Reproductive System Disease
257. Familial Paraganglioma
[An inherited neoplasm arising from paraganglia. The majority of cases (up to 80%) are multifocal. ( NCI )] (UMLS (NCI) C1333993) Hereditary Paraganglioma =Neoplastic Process ;
208. False Vocal Cord
(UMLS (NCI) C0149596) =Body Part, Organ, or Organ Component
258. familial periodic paralysis
[heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia; these conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle; frequently associated with fluctuations in serum potassium levels; periodic paralysis may also occur as a non-familial process secondary to thyrotoxicosis and other conditions. ( CSP )] (UMLS (CSP) C0030443) =Disease or Syndrome ;
=inborn metal metabolism disorder;
muscle disorder;
DISORDERS OF THE PERIPHERAL NERVOUS SYSTEM;
=Paralysis, Hyperkalemic Periodic;
Hypokalemic Periodic Paralysis
209. Falx Cerebelli
(UMLS (NCI) C0228122) =Body Part, Organ, or Organ Component
259. FAMILIAL POLYCYTHEMIA
(UMLS (ICD9CM) C0152264) =Disease or Syndrome ;
210. FAM HX DIGEST DISORD NEC
(UMLS (ICD9CM) C1719679) Other digestive disorders =Disease or Syndrome
260. familial progressive polyneuropathy
[ ] (UMLS (CSP) C0598588) =Pathologic Function
211. FAM HX GENET DIS CARRIER
[an individual who is heterozygous for a recessive gene and thus does not express the recessive phenotype but can transmit the gene to offspring. ( CSP )] (UMLS (ICD9CM) C0007294) =Patient or Disabled Group =family genetics;
261. Familial Renal Oncocytoma
(UMLS (NCI) C0879606) Hereditary Renal Oncocytoma =Neoplastic Process
212. FAM HX MEN SYNDROME
[ ] (UMLS (ICD9CM) C1955576) Multiple endocrine neoplasia [MEN] syndrome;
=Finding
262. Familial Renal Papillary Carcinoma
(UMLS (NCI) C0879257) Hereditary Kidney Papillary Carcinoma;
Hereditary Papillary Carcinoma of Kidney;
Hereditary Papillary Carcinoma of the Kidney;
Hereditary Papillary Renal Carcinoma;
Hereditary Papillary Renal Cell Carcinoma;
=Neoplastic Process
213. FAM HX SUDDEN CARD DEATH
[ ] (UMLS (ICD9CM) C1955575) Family history of sudden cardiac death (SCD);
=Disease or Syndrome
263. Familial Retinoblastoma
(UMLS (NCI) C0751483) Hereditary Retinoblastoma =Neoplastic Process
214. FAM HX-BLADDER MALIG
[ ] (UMLS (ICD9CM) C1955574) Family history of malignant neoplasm of bladder;
=Disease or Syndrome
264. familial splenic anemia
[autosomal recessive disorder caused by deficiency of the enzyme glucocerebrosidase featuring the pathological storage of glycosylceramide in mononuclear phagocytes; the most common subtype is the non-neuronopathic form, a slowly progressive condition characterized by hepatosplenomegaly and skeletal deformities; the neuronopathic forms are divided into infantile and juvenile forms; the infantile form presents at 4-5 months of age with anemia, loss of cognitive gains, neck retraction, dysphagia, and hepatosplenomegaly; the juvenile form features a slowly progressive loss of intellect, hepatosplenomegaly, ataxia, myoclonic seizures, and spasticity; the neuronopathic forms are characterized by neuronal loss with neuronophagia, and accumulation of glucocerebroside in neurons. ( CSP )] (UMLS (CSP) C0017205) =Disease or Syndrome ;
=Arrieration mentale;
Reticuloendothelial Hyperplasia;
Sphingolipidoses;
enzyme deficiency
215. FAM HX-BLOOD DISORD NEC
[ ] (UMLS (ICD9CM) C0260529) =Finding
265. Familial Wilms' Tumor
[Familial embryonal neoplasm derived from nephrogenic blastemal cells. Several lines of differentiation, including blastemal, stromal and epithelial, are usually expressed. Comprises approximately 1% of Wilms' tumors. (AFIP fascicle version 2.0 mo011000) ( NCI )] (UMLS (NCI) C0677779) =Neoplastic Process
216. FAM HX-CARDIOVAS DIS NEC
[ ] (UMLS (ICD9CM) C1963707) Family history of other cardiovascular diseases;
=Finding ;
266. Familiar Atypical Multiple Mole
(UMLS (NCI) C0015565) =Finding
217. FAM HX-CHR RESP COND NEC
[ ] (UMLS (ICD9CM) C0260523) =Finding
267. Familiar Dystonia
(UMLS (NCI) C0752207) =Disease or Syndrome
218. FAM HX-CONGEN ANOMALIES
[ ] (UMLS (ICD9CM) C0260541) =Finding
268. Familiar Female Breast Carcinoma
(UMLS (NCI) C1333986) Hereditary Female Breast Carcinoma =Neoplastic Process ;
219. FAM HX-DIABETES MELLITUS
[ ] (UMLS (ICD9CM) C0260526) =Finding
269. Familiar Idiopathic Dystonia
(UMLS (NCI) C0393598) =Disease or Syndrome
220. FAM HX-INTRATHORACIC MAL
[ ] (UMLS (ICD9CM) C0260508) =Finding
270. Familiar Male Breast Carcinoma
(UMLS (NCI) C1333988) Hereditary Male Breast Carcinoma =Neoplastic Process ;
221. FAM HX-ISCHEM HEART DIS
[ ] (UMLS (ICD9CM) C0260520) =Finding
271. Familiar Neoplastic Syndrome
[The inherited predisposition toward getting a cancer ( NCI )] (UMLS (NCI) C0027672) =Neoplastic Process =Genetic Condition;
KASVAIMET =Colorectal Neoplasms, Hereditary Nonpolyposis;
Atypical Mole Syndrome;
Gardner Syndrome;
Cowden Syndrome;
MEA;
Jeghers-Peutz Syndrome;
Adenomatous Polyposis Coli;
Encephalotrigeminal Syndrome;
Li Fraumeni syndrome;
neurofibromatoses
222. FAM HX-KIDNEY DIS NEC
[ ] (UMLS (ICD9CM) C0695259) =Finding
272. Familiar Ovarian Carcinoma
(UMLS (NCI) C1333992) Hereditary Ovarian Carcinoma =Neoplastic Process ;
223. FAM HX-LYMPH NEOPLAS NEC
[ ] (UMLS (ICD9CM) C0260513) =Finding
273. Family
(UMLS (HL7) C1563343) =Idea or Concept ;
=Living Arrangement;
◊ (UMLS (HL7) C1552262) Professional or Occupational Group Nurse Practitioner;
224. FAM HX-MENTAL RETARDAT
[ ] (UMLS (ICD9CM) C0260530) =Finding
274. family
[Family name, this is the name that links to the genealogy. In some cultures (e.g. Eritrea) the family name of a son is the first name of his father. ( HL7V3.0 )] (UMLS (HL7) C1546847) =Idea or Concept =EntityNamePartType;
225. FAM HX-NEUROLOG DIS NEC
[ ] (UMLS (ICD9CM) C0260519) =Finding
275. Family
(UMLS (HL7) C1555907) =Professional or Occupational Group =Psychologist;
226. FAM HX-POLYCYSTIC KIDNEY
[ ] (UMLS (ICD9CM) C0455422) =Finding
276. family ataxia
[inherited disease with degenerative changes in the dorsal half of spinal cord and cerebellum; characterized by ataxia of extremities and trunk, speech impairment, and lateral curvature of the spine. ( CSP )] (UMLS (CSP) C0016719) =Disease or Syndrome ;
=Cerebellar Diseases;
Genetic Condition;
Spinocerebellar Degenerations;
227. FAM HX-PSYCHIATRIC COND
[ ] (UMLS (ICD9CM) C0260517) =Finding
277. Family Cancer History
[A record of a patient's medical background regarding the cancer and cancer-related problems of blood relatives. ( NCI )] (UMLS (NCI) C0260515) =Finding
228. FAM HX-URINRY MALIG NEC
(UMLS (ICD9CM) C0700059) =Finding
278. FAMILY CIRCUMSTANCE NOS
[ ] (UMLS (ICD9CM) C0029795) =Finding ;
229. FAM MEDITERRANEAN FEVER
[An autosomal recessive inherited disease characterized by episodic FEVER; severe ABDOMINAL PAIN; PLEURISY; ARTHRITIS; and a characteristic ankle RASH. Disease flare-ups tend to last 3 days, and individuals are asymptomatic between attacks. ORCHITIS; benign recurrent MENINGITIS; HEADACHE; and AMYLOID nephropathy may also occur. (From Medicine (Baltimore) 1998 Jul;77(4):268-97) ( MSH )] (UMLS (ICD9CM) C0031069) =Disease or Syndrome ;
=Hypothalamic Diseases;
279. FAMILY CIRCUMSTANCES NEC
[ ] (UMLS (ICD9CM) C0481799) =Finding
230. FAMCICLOVIR
[A diacetyl 6-deoxy prodrug analog of the antiviral agent penciclovir. Orally administered, famciclovir in vivo is converted to penciclovir triphosphate, which is active against the Herpes viruses, including herpes simplex 1 and 2 and varicella-zoster. This agent inhibits the replication of viral DNA by interfering competitively with DNA polymerase. (NCI04) ( NCI )] (UMLS (NCI) C0209227) =Organic Chemical; Pharmacologic Substance =2-Aminopurine;
[AM800] ANTIVIRALS =FAMCICLOVIR 125 MG;
FAMCICLOVIR 250 MG;
FAMCICLOVIR 500 MG;
280. family dependent
[The player of the role is dependent of the scoping entity. ( HL7V3.0 )] (UMLS (HL7) C1552576) =Intellectual Product =CoverageRoleType;
231. FAMIL HERED DIS-ANTEPART
[ ] (UMLS (ICD9CM) C0157075) =Disease or Syndrome
281. FAMILY DISRUPTION
[ ] (UMLS (ICD9CM) C0481798) =Finding
232. FAMIL HEREDIT DIS-DELIV
[ ] (UMLS (ICD9CM) C0157074) =Disease or Syndrome
282. family dynamics
[composition of a family unit and interaction of the individual members with each other and as a unit. ( CSP )] (UMLS (CSP) C0015609) =Social Behavior =Familial;
=parent child interaction;
233. FAMIL HEREDIT DIS-UNSPEC
[ ] (UMLS (ICD9CM) C0157073) =Disease or Syndrome ;
283. family genetics
[index on studies of possible genetic transmission of disease or other phenotypes within families. ( CSP )] (UMLS (CSP) C0599775) =Occupation or Discipline ;
=human population genetics;
=FAM HX GENET DIS CARRIER
234. Familial
[group of individuals related by blood or marriage or other arrangements, including parents or parent substitutes and children, however, the specific members differ from culture to culture. ( CSP )] (UMLS (NCI) C0015576) =Family Group =ethology;
sociology/anthropology =child rearing;
unwanted child;
family dynamics;
family size;
household;
Parent;
Sib;
Spouse;
grandparent;
marriage/marital status
284. Family Health
(UMLS (HL7) C1552233) =Professional or Occupational Group =Clinical Nurse Specialist;
235. Familial Adenomatous Polyposis Associated Medulloblastoma
[A medulloblastoma developing in patients with familiar adenomatous polyposis syndrome. It is observed in patients with Turcot syndrome, type 2. ( NCI )] (UMLS (NCI) C1333598) FAP Associated Medulloblastoma;
=Neoplastic Process
285. Family Health Care Professional
(UMLS (HL7) C1547430) =Professional or Occupational Group =Provider role;
236. Familial Atypical Mole Melanoma Syndrome
(UMLS (NCI) C0205747) =Neoplastic Process
286. FAMILY HEALTH PROBL NEC
[ ] (UMLS (ICD9CM) C0260804) =Finding
237. Familial Breast Carcinoma
(UMLS (NCI) C0346153) =Neoplastic Process
287. Family history of allergic disorders
[ ] (UMLS (ICD9CM) C0260542) =Finding
238. Familial Breast/Ovarian Cancer (BRCA1, BRCA2)
(UMLS (NCI) C0677776) =Neoplastic Process
288. Family history of anemia
[ ] (UMLS (ICD9CM) C0260528) =Finding
239. familial cancer
[Cancer that occurs in families more often than would be expected by chance. These cancers often occur at an early age, and may indicate the presence of a gene mutation that increases the risk of cancer. They may also be a sign of shared environmental or lifestyle factors. ( NCI )] (UMLS (NCI) C1333600) Familiar Malignant Neoplasm;
Hereditary Cancer;
Hereditary Malignant Neoplasm;
=Neoplastic Process
289. Family history of arthritis
(UMLS (ICD9CM) C0221565) =Finding ;
240. familial cholesteryl ester deficiency
[disease characterized by abnormally low levels of plasma lecithin cholesterol acyl transferase; clinical manifestations include corneal opacity, anemia, and proteinuria. ( CSP )] (UMLS (CSP) C0023195) =Disease or Syndrome ;
=hypolipoproteinemia;
enzyme deficiency;
familial hypolipoproteinemia;
290. Family history of asthma
[ ] (UMLS (ICD9CM) C0260522) =Finding
241. familial disorder
[ ] (UMLS (CSP) C0277558) =Disease or Syndrome
291. Family history of blindness or visual loss
(UMLS (ICD9CM) C0496709) =Finding
242. familial erythroblastic anemia
[ ] (UMLS (CSP) C0599527) =Disease or Syndrome ;
292. Family history of certain chronic disabling diseases
[ ] (UMLS (ICD9CM) C0260516) =Finding
243. familial fat induced hyperlipemia
[ ] (UMLS (CSP) C0598426) =Disease or Syndrome ;
293. Family history of certain other specific conditions
[ ] (UMLS (ICD9CM) C0260525) =Finding
244. Familial Glomangioma
[A familial glomus tumor. ( NCI )] (UMLS (NCI) C1333987) Hereditary Glomangioma =Neoplastic Process ;
294. Family history of deafness or hearing loss
[ ] (UMLS (ICD9CM) C0260538) =Finding
245. familial hemophagocytic lymphohistiocytosis
[Rare form of hemophagocytic lymphohistiocytosis with multiorgan involvement seen in infants and young children ( MSH )] (UMLS (CSP) C0272199) =Neoplastic Process
295. Family history of digestive disorders
(UMLS (ICD9CM) C0496716) =Finding
246. familial high density lipoprotein deficiency
[ ] (UMLS (CSP) C1704429) =Disease or Syndrome ;
296. Family history of infectious and parasitic diseases
[ ] (UMLS (ICD9CM) C0260534) =Finding
247. familial hyperbetalipoproteinemia
[characterized by increased plasma concentration of cholesterol carried in low density lipoproteins (LDL) and by a deficiency in a cell surface receptor which regulates LDL degradation and cholesterol synthesis. ( CSP )] (UMLS (CSP) C0020445) =Disease or Syndrome =hypercholesteremia;
Hyperlipidemia, Familial Combined;
familial hyperlipoproteinemia;
297. Family history of kidney diseases
[ ] (UMLS (ICD9CM) C1261328) =Finding ;
248. familial hyperlipemia
[ ] (UMLS (CSP) C0694546) =Disease or Syndrome
298. Family history of leukemia
[ ] (UMLS (ICD9CM) C0260512) =Finding
249. familial hyperlipoproteinemia
[group of disorders genetically distinct from the other inherited hyperlipidemias classified on the basis of type I through V phenotypes; see narrower terms. ( CSP )] (UMLS (CSP) C0700623) =Disease or Syndrome ;
=hyperlipoproteinemia;
inborn lipid/lipoprotein disorder =familial hyperbetalipoproteinemia;
broad beta disease;
familial hyperlipoproteinemia type IV;
Burger Grutz syndrome;
299. Family history of malignant neoplasm
[ ] (UMLS (ICD9CM) C1261378) Family history of unspecified malignant neoplasm;
FAMILY HX-MALIGNANCY NOS =Finding ;
250. familial hyperlipoproteinemia type IV
[characterized by an isolated elevation in the plasma level of endogenously synthesized triglyceride carried in VLDL; considered to be an autosomal dominant trait. ( CSP )] (UMLS (CSP) C0020480) =Disease or Syndrome =Hyperlipidemia, Familial Combined;
familial hyperlipoproteinemia
300. Family history of malignant neoplasm of breast
[ ] (UMLS (ICD9CM) C1261325) FAMILY HX-BREAST MALIG =Finding ;

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