- 301. Fallopian Tube Non-Neoplastic Disease
- (UMLS (NCI) C1333594) Fallopian Tube Non-Neoplastic Disorder;
=Disease or Syndrome | - 351. 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 |
- 302. FALLOPIAN TUBE OP NEC
- [ ] (UMLS (ICD9CM) C0175610) =Therapeutic or Preventive Procedure
| - 352. 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;
|
- 303. Fallopian Tube Papillary Adenocarcinoma
- (UMLS (NCI) C1333595) Papillary Adenocarcinoma of Fallopian Tube;
Papillary Adenocarcinoma of the Fallopian Tube =Neoplastic Process | - 353. 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 |
- 304. Fallopian Tube Squamous Cell Carcinoma
- (UMLS (NCI) C1333596) Squamous Cell Carcinoma of Fallopian Tube;
Squamous Cell Carcinoma of the Fallopian Tube =Neoplastic Process | - 354. 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;
|
- 305. 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 | - 355. 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;
|
- 306. False Alarm
- [A test result that shows evidence of a result or condition although it is not actually present. ( NCI )] (UMLS (NCI) C0205557) =Finding
| - 356. familial hypothyroidism
- [inherited deficiency of thyroid gland activity. ( CSP )] (UMLS (CSP) C0596558) =Disease or Syndrome =Genetic Condition;
hypothyroidism |
- 307. FALSE POS SERO TEST-SYPH
- [ ] (UMLS (ICD9CM) C0159128) =Finding
| - 357. Familial Meningioma
- (UMLS (NCI) C1333989) Hereditary Meningioma =Neoplastic Process ;
|
- 308. 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 | - 358. 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 ;
|
- 309. False Vocal Cord
- (UMLS (NCI) C0149596) =Body Part, Organ, or Organ Component
| - 359. 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 |
- 310. Falx Cerebelli
- (UMLS (NCI) C0228122) =Body Part, Organ, or Organ Component
| - 360. FAMILIAL POLYCYTHEMIA
- (UMLS (ICD9CM) C0152264) =Disease or Syndrome ;
|
- 311. FAM HX DIGEST DISORD NEC
- (UMLS (ICD9CM) C1719679) Other digestive disorders =Disease or Syndrome
| - 361. familial progressive polyneuropathy
- [ ] (UMLS (CSP) C0598588) =Pathologic Function
|
- 312. 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;
| - 362. Familial Renal Oncocytoma
- (UMLS (NCI) C0879606) Hereditary Renal Oncocytoma =Neoplastic Process
|
- 313. FAM HX MEN SYNDROME
- [ ] (UMLS (ICD9CM) C1955576) Multiple endocrine neoplasia [MEN] syndrome;
=Finding | - 363. 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 |
- 314. FAM HX SUDDEN CARD DEATH
- [ ] (UMLS (ICD9CM) C1955575) Family history of sudden cardiac death (SCD);
=Disease or Syndrome | - 364. Familial Retinoblastoma
- (UMLS (NCI) C0751483) Hereditary Retinoblastoma =Neoplastic Process
|
- 315. FAM HX-BLADDER MALIG
- [ ] (UMLS (ICD9CM) C1955574) Family history of malignant neoplasm of bladder;
=Disease or Syndrome | - 365. 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 |
- 316. FAM HX-BLOOD DISORD NEC
- [ ] (UMLS (ICD9CM) C0260529) =Finding
| - 366. 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
|
- 317. FAM HX-CARDIOVAS DIS NEC
- [ ] (UMLS (ICD9CM) C1963707) Family history of other cardiovascular diseases;
=Finding ;
| - 367. Familiar Atypical Multiple Mole
- (UMLS (NCI) C0015565) =Finding
|
- 318. FAM HX-CHR RESP COND NEC
- [ ] (UMLS (ICD9CM) C0260523) =Finding
| - 368. Familiar Dystonia
- (UMLS (NCI) C0752207) =Disease or Syndrome
|
- 319. FAM HX-CONGEN ANOMALIES
- [ ] (UMLS (ICD9CM) C0260541) =Finding
| - 369. Familiar Female Breast Carcinoma
- (UMLS (NCI) C1333986) Hereditary Female Breast Carcinoma =Neoplastic Process ;
|
- 320. FAM HX-DIABETES MELLITUS
- [ ] (UMLS (ICD9CM) C0260526) =Finding
| - 370. Familiar Idiopathic Dystonia
- (UMLS (NCI) C0393598) =Disease or Syndrome
|
- 321. FAM HX-INTRATHORACIC MAL
- [ ] (UMLS (ICD9CM) C0260508) =Finding
| - 371. Familiar Male Breast Carcinoma
- (UMLS (NCI) C1333988) Hereditary Male Breast Carcinoma =Neoplastic Process ;
|
- 322. FAM HX-ISCHEM HEART DIS
- [ ] (UMLS (ICD9CM) C0260520) =Finding
| - 372. 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 |
- 323. FAM HX-KIDNEY DIS NEC
- [ ] (UMLS (ICD9CM) C0695259) =Finding
| - 373. Familiar Ovarian Carcinoma
- (UMLS (NCI) C1333992) Hereditary Ovarian Carcinoma =Neoplastic Process ;
|
- 324. FAM HX-LYMPH NEOPLAS NEC
- [ ] (UMLS (ICD9CM) C0260513) =Finding
| - 374. Family
- (UMLS (HL7) C1563343) =Idea or Concept ;
=Living Arrangement;
◊ (UMLS (HL7) C1552262) Professional or Occupational Group Nurse Practitioner; |
- 325. FAM HX-MENTAL RETARDAT
- [ ] (UMLS (ICD9CM) C0260530) =Finding
| - 375. 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;
|
- 326. FAM HX-NEUROLOG DIS NEC
- [ ] (UMLS (ICD9CM) C0260519) =Finding
| - 376. Family
- (UMLS (HL7) C1555907) =Professional or Occupational Group =Psychologist;
|
- 327. FAM HX-POLYCYSTIC KIDNEY
- [ ] (UMLS (ICD9CM) C0455422) =Finding
| - 377. 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;
|
- 328. FAM HX-PSYCHIATRIC COND
- [ ] (UMLS (ICD9CM) C0260517) =Finding
| - 378. 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
|
- 329. FAM HX-URINRY MALIG NEC
- (UMLS (ICD9CM) C0700059) =Finding
| - 379. FAMILY CIRCUMSTANCE NOS
- [ ] (UMLS (ICD9CM) C0029795) =Finding ;
|
- 330. 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;
| - 380. FAMILY CIRCUMSTANCES NEC
- [ ] (UMLS (ICD9CM) C0481799) =Finding
|
- 331. 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;
| - 381. family dependent
- [The player of the role is dependent of the scoping entity. ( HL7V3.0 )] (UMLS (HL7) C1552576) =Intellectual Product =CoverageRoleType;
|
- 332. FAMIL HERED DIS-ANTEPART
- [ ] (UMLS (ICD9CM) C0157075) =Disease or Syndrome
| - 382. FAMILY DISRUPTION
- [ ] (UMLS (ICD9CM) C0481798) =Finding
|
- 333. FAMIL HEREDIT DIS-DELIV
- [ ] (UMLS (ICD9CM) C0157074) =Disease or Syndrome
| - 383. 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;
|
- 334. FAMIL HEREDIT DIS-UNSPEC
- [ ] (UMLS (ICD9CM) C0157073) =Disease or Syndrome ;
| - 384. 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 |
- 335. 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 | - 385. Family Health
- (UMLS (HL7) C1552233) =Professional or Occupational Group =Clinical Nurse Specialist;
|
- 336. 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 | - 386. Family Health Care Professional
- (UMLS (HL7) C1547430) =Professional or Occupational Group =Provider role;
|
- 337. Familial Atypical Mole Melanoma Syndrome
- (UMLS (NCI) C0205747) =Neoplastic Process
| - 387. FAMILY HEALTH PROBL NEC
- [ ] (UMLS (ICD9CM) C0260804) =Finding
|
- 338. Familial Breast Carcinoma
- (UMLS (NCI) C0346153) =Neoplastic Process
| - 388. Family history of allergic disorders
- [ ] (UMLS (ICD9CM) C0260542) =Finding
|
- 339. Familial Breast/Ovarian Cancer (BRCA1, BRCA2)
- (UMLS (NCI) C0677776) =Neoplastic Process
| - 389. Family history of anemia
- [ ] (UMLS (ICD9CM) C0260528) =Finding
|
- 340. 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 | - 390. Family history of arthritis
- (UMLS (ICD9CM) C0221565) =Finding ;
|
- 341. 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;
| - 391. Family history of asthma
- [ ] (UMLS (ICD9CM) C0260522) =Finding
|
- 342. familial disorder
- [ ] (UMLS (CSP) C0277558) =Disease or Syndrome
| - 392. Family history of blindness or visual loss
- (UMLS (ICD9CM) C0496709) =Finding
|
- 343. familial erythroblastic anemia
- [ ] (UMLS (CSP) C0599527) =Disease or Syndrome ;
| - 393. Family history of certain chronic disabling diseases
- [ ] (UMLS (ICD9CM) C0260516) =Finding
|
- 344. familial fat induced hyperlipemia
- [ ] (UMLS (CSP) C0598426) =Disease or Syndrome ;
| - 394. Family history of certain other specific conditions
- [ ] (UMLS (ICD9CM) C0260525) =Finding
|
- 345. Familial Glomangioma
- [A familial glomus tumor. ( NCI )] (UMLS (NCI) C1333987) Hereditary Glomangioma =Neoplastic Process ;
| - 395. Family history of deafness or hearing loss
- [ ] (UMLS (ICD9CM) C0260538) =Finding
|
- 346. familial hemophagocytic lymphohistiocytosis
- [Rare form of hemophagocytic lymphohistiocytosis with multiorgan involvement seen in infants and young children ( MSH )] (UMLS (CSP) C0272199) =Neoplastic Process
| - 396. Family history of digestive disorders
- (UMLS (ICD9CM) C0496716) =Finding
|
- 347. familial high density lipoprotein deficiency
- [ ] (UMLS (CSP) C1704429) =Disease or Syndrome ;
| - 397. Family history of infectious and parasitic diseases
- [ ] (UMLS (ICD9CM) C0260534) =Finding
|
- 348. 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;
| - 398. Family history of kidney diseases
- [ ] (UMLS (ICD9CM) C1261328) =Finding ;
|
- 349. familial hyperlipemia
- [ ] (UMLS (CSP) C0694546) =Disease or Syndrome
| - 399. Family history of leukemia
- [ ] (UMLS (ICD9CM) C0260512) =Finding
|
- 350. 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;
| - 400. Family history of malignant neoplasm
- [ ] (UMLS (ICD9CM) C1261378) Family history of unspecified malignant neoplasm;
FAMILY HX-MALIGNANCY NOS =Finding ;
|
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