- 201. JT STIFFNES NEC-FOREARM
- [ ] (UMLS (ICD9CM) C0158198) =Disease or Syndrome
| - 239. just noticeably different
- [ ] (UMLS (CSP) C1537025) =Mental Process
|
- 202. JT STIFFNESS NEC-ANKLE
- [ ] (UMLS (ICD9CM) C0158202) =Disease or Syndrome
| - 240. justify
- (UMLS (HL7) C1552821) =Functional Concept =TableCellHorizontalAlign;
|
- 203. JT STIFFNESS NEC-HAND
- [ ] (UMLS (ICD9CM) C0158199) =Disease or Syndrome
| - 241. JUV EPITH CORNEA DYSTRPH
- [An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder. ( MSH )] (UMLS (ICD9CM) C0339277) =Congenital Abnormality ;
|
- 204. JT STIFFNESS NEC-L/LEG
- [ ] (UMLS (ICD9CM) C0158201) =Disease or Syndrome
| - 242. JUV OSTEOCHONDROS PELVIS
- (UMLS (ICD9CM) C0022441) =Disease or Syndrome
|
- 205. JT STIFFNESS NEC-MULT JT
- [ ] (UMLS (ICD9CM) C0158204) =Disease or Syndrome
| - 243. JUV OSTEOCHONDROS SPINE
- [Osteochondrosis of the vertebral epiphyses in children. ( MSH )] (UMLS (ICD9CM) C0036310) =Disease or Syndrome =osteochondritis;
DORSOPATHIES |
- 206. JT STIFFNESS NEC-OTH JT
- [ ] (UMLS (ICD9CM) C0158203) =Disease or Syndrome
| - 244. JUV OSTEOCHONDROSIS ARM
- [ ] (UMLS (ICD9CM) C0158442) =Disease or Syndrome
|
- 207. JT STIFFNESS NEC-PELVIS
- [ ] (UMLS (ICD9CM) C0158200) =Disease or Syndrome
| - 245. JUV OSTEOCHONDROSIS FOOT
- [ ] (UMLS (ICD9CM) C0158444) =Disease or Syndrome
|
- 208. JT STIFFNESS NEC-SHLDER
- [ ] (UMLS (ICD9CM) C0158196) =Disease or Syndrome
| - 246. JUV OSTEOCHONDROSIS LEG
- [ ] (UMLS (ICD9CM) C1282912) Juvenile osteochondrosis of lower extremity, excluding foot;
=Disease or Syndrome |
- 209. JT STIFFNESS NEC-UNSPEC
- [ ] (UMLS (ICD9CM) C0158195) =Disease or Syndrome
| - 247. JUV OSTEOCHONDROSIS NEC
- [ ] (UMLS (ICD9CM) C0158445) =Disease or Syndrome
|
- 210. JT STIFFNESS NEC-UP/ARM
- [ ] (UMLS (ICD9CM) C0158197) =Disease or Syndrome
| - 248. JUV RHEUM ARTHRITIS NOS
- [ ] (UMLS (ICD9CM) C0837691) Polyarticular juvenile rheumatoid arthritis, chronic or unspecified =Disease or Syndrome
|
- 211. JTB
- [Jumping translocation (JT) is an unbalanced translocation that comprises amplified chromosomal segments jumping to various telomeres. The JTB gene (jumping translocation breakpoint) is found fused with the telomeric repeats of acceptor telomeres in a case of jumping translocation. Jumping Translocation Breakpoint is encoded by this open reading frame, and is highly conserved among divergent eukaryotic species. JTB is a 146-aa protein with a 75-aa extracellular domain, a 21-aa transmembrane domain, and a 20-aa intracellular domain. Jumping translocations have been reported in leukemia patients, in the Ewing family of tumors, in renal clear cell carcinoma, and in liposarcoma. (from OMIM) ( NCI )] (UMLS (NCI) C0914182) JTB Protein;
Jumping Translocation Breakpoint Protein;
PAR Protein;
Prostate Androgen Regulated Protein =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
| - 249. Juven
- [An orally bioavailable nutritional supplement. Juven contains the amino acids glutamine and arginine in addition to beta-hydroxy-beta-methylbutyrate (HMB). This agent may promote muscle protein synthesis and increase muscle mass. (NCI04) ( NCI )] (UMLS (NCI) C0939574) =Food ;
|
- 212. JTB
- [This gene is involved in the regulation of telomeric repeats and jumping translocation. The gene is also associated with different types of leukemia. ( NCI )] (UMLS (NCI) C1334294) JTB Gene;
Jumping Translocation Breakpoint Gene;
=Gene or Genome ;
| - 250. JUVEN DERMAT HERPETIFORM
- [ ] (UMLS (ICD9CM) C0152092) =Disease or Syndrome
|
- 213. JTK14
- [Specifically expressed in developing endothelial cells by human TIE Gene (TIE Tyr Kinase Family), 1138-aa 125-kDa (precursor) type I transmembrane Protein Receptor Tyrosine Kinase TIE 1 contains 2 Ig-like C2-type domains, 3 fibronectin type III domains, and 3 EGF-like domains. TIE1 receptor may be involved in multiple protein-protein interactions, possibly including endothelial cell adhesion, blood clotting, and inflammation. TIE1 receptor is important in angiogenesis, particularly endothelial vascular formation. Combinatorial ANG-1 and TIE1 orphan receptor function is critical for right-side venous system development. (NCI) ( NCI )] (UMLS (NCI) C1335549) Protein Receptor Tyrosine Kinase TIE 1;
TIE1;
Tyrosine Kinase with Immunoglobulin and Epidermal Growth Factor Homology Domains;
Tyrosine-Protein Kinase Receptor TIE1;
=Amino Acid, Peptide, or Protein; Enzyme; Receptor | - 251. juvenile animal
- [animal between infancy and adulthood. ( CSP )] (UMLS (CSP) C0598744) =Animal ;
=immature animal;
|
- 214. judgment
- [process of discovering or asserting an objective or intrinsic relation between two objects or concepts; a faculty or power that enables a person to make judgments; the process of bringing to light and asserting the implicit meaning of a concept; a critical evaluation of a person or situation. ( CSP )] (UMLS (CSP) C0022423) =Mental Process ;
=cognition;
| - 252. Juvenile Breast Papillomatosis
- (UMLS (NCI) C1334303) Juvenile Papillomatosis of Breast;
Juvenile Papillomatosis of the Breast;
=Neoplastic Process |
- 215. Jug
- [A deep vessel for holding liquids, with a handle and often with a spout or lip shape for pouring. ( HL7V3.0 )] (UMLS (HL7) C1553462) =Intellectual Product =MultiUseContainerEntityType;
| - 253. Juvenile Cataract
- (UMLS (NCI) C0302254) =Anatomical Abnormality
|
- 216. jugular body
- [A highly vascular ovoid body of chemoreceptive tissue lying adjacent to the TYMPANIC CAVITY. It is derived from NEURAL CREST tissue and is considered part of the diffuse neuroendocrine system. It is the site of a rare neoplasm called a GLOMUS TYMPANICUM TUMOR. ( MSH )] (UMLS (CSP) C0205878) =Body Part, Organ, or Organ Component ;
| - 254. Juvenile chronic polyarthritis
- [ ] (UMLS (ICD9CM) C0409667) =Disease or Syndrome
|
- 217. Jugular Foramen
- (UMLS (NCI) C0222712) =Body Space or Junction
| - 255. juvenile delinquency
- [antisocial behavior by youths which is subject to legal sanctions. ( CSP )] (UMLS (CSP) C0022438) =Individual Behavior =child behavior disorder;
social disturbance |
- 218. Jugular Foramen Meningioma
- (UMLS (NCI) C1334298) Meningioma of Jugular Foramen;
Meningioma of the Jugular Foramen;
=Neoplastic Process | - 256. juvenile hormone
- [natural or synthetic compounds which prevent metamorphosis in the growing insect. ( CSP )] (UMLS (CSP) C0022439) =Hormone =Fatty Acids, Unsaturated;
invertebrate hormone |
- 219. Jugular Foramen Neoplasm
- (UMLS (NCI) C1334299) Jugular Foramen Neoplasms;
Jugular Foramen Tumor;
Jugular Foramen Tumors;
Neoplasm of Jugular Foramen;
Neoplasm of the Jugular Foramen;
Tumor of Jugular Foramen;
Tumor of the Jugular Foramen =Neoplastic Process | - 257. Juvenile Multiple Polyps Syndrome
- (UMLS (NCI) C0345893) =Neoplastic Process
|
- 220. Jugular Foramen Neurilemmoma
- (UMLS (NCI) C1334300) Jugular Foramen Schwannoma;
Neurilemmoma of Jugular Foramen;
Neurilemmoma of the Jugular Foramen;
Schwannoma of Jugular Foramen;
Schwannoma of the Jugular Foramen =Neoplastic Process | - 258. juvenile myoclonic epilepsy
- [A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323) ( MSH )] (UMLS (CSP) C0270853) =Disease or Syndrome =Epilepsies, Myoclonic;
|
- 221. jugular vein
- [veins in the neck which drain the brain, face, and neck into the brachiocephalic or subclavian veins. ( CSP )] (UMLS (CSP) C0022427) =Body Part, Organ, or Organ Component ;
=vein;
cerebrovascular system | - 259. JUVENILE NEUROSYPH NEC
- [ ] (UMLS (ICD9CM) C0153135) =Disease or Syndrome
|
- 222. Jugular, Internal
- (UMLS (HL7) C1550269) =Body Part, Organ, or Organ Component =Body Part;
| - 260. JUVENILE NEUROSYPH NOS
- [ ] (UMLS (ICD9CM) C0153132) =Disease or Syndrome
|
- 223. Juice
- (UMLS (NCI) C1268568) =Food; ;
| - 261. Juvenile Osteochondrosis
- (UMLS (NCI) C0729346) =Disease or Syndrome ;
|
- 224. Juice Plus
- (UMLS (NCI) C1328004) =Food ;
| - 262. juvenile periodontitis
- [Localized periodontitis in teenagers and young adults. The onset is during the circumpubertal period but the diagnosis can be made beyond puberty. Lesions are confined predominantly to the first permanent molars or incisors and the distribution of lesions is usually symmetrical. The gingiva may appear normal. The lesions are highly active immediately following puberty but later destruction may slow or cease spontaneously. The disease is four times more prevalent in females than males and more prevalent in African Americans than in other races or ethnic groups. (From Schluger et al., Periodontal Diseases, 2d ed, p61) ( MSH )] (UMLS (CSP) C0031106) =Disease or Syndrome ;
=Chronic Periodontitis;
|
- 225. JUN
- [An oncogene from an avian sarcoma virus. The protein it encodes dimerizes with fos to form the transcription factor AP1. ( NCI )] (UMLS (NCI) C0162508) =Gene or Genome
| - 263. Juvenile Pilocytic Astrocytoma
- (UMLS (NCI) C0280783) =Neoplastic Process
|
- 226. JUN B Proto-Oncogene Gene
- [This gene plays a role in transcriptional regulation and myelopoiesis. ( NCI )] (UMLS (NCI) C0812313) JUNB;
JUNB Gene =Gene or Genome ;
| - 264. Juvenile Polyp
- (UMLS (NCI) C0221273) =Neoplastic Process ;
|
- 227. JUN D Proto-oncogene Gene
- [This gene plays a role in transcriptional regulation, apoptotic responses to cellular stress and signal transduction pathways. ( NCI )] (UMLS (NCI) C0812312) JUND;
JUND Gene =Gene or Genome ;
| - 265. Juvenile Polyp of Rectum
- (UMLS (NCI) C1335680) Juvenile Polyp of the Rectum;
Rectal Juvenile Polyp =Disease or Syndrome ;
|
- 228. JUN kinase
- [a stress activated protein kinase. ( CSP )] (UMLS (CSP) C0872053) =Amino Acid, Peptide, or Protein; Enzyme =EC 2.7;
| - 266. Juvenile Type Granulosa Cell Neoplasm
- [A granulosa cell tumor occurring in the ovary and testis. In females it occurs predominantly in the first three decades of life and presents unilaterally as stage I disease in the vast majority of cases. It is characterized by the presence of granulosa cells forming macrofollicular structures. The majority of cases have a good prognosis. In males it represents the most frequent congenital testicular neoplasm and the vast majority of cases occur in the perinatal period. It presents as a scrotal or abdominal mass and it more often affects the left testis. Approximately 20% of the patients have ambiguous external genitalia. It is characterized by the presence of cystic spaces lined by granulosa cells and cells resembling theca cells. Metastases have not been reported. ( NCI )] (UMLS (NCI) C0334403) =Neoplastic Process
|
- 229. Junction Plakoglobin Gene
- [This gene is involved in cellular adhesion and modulates cadherin interactions. ( NCI )] (UMLS (NCI) C1334295) JUP;
JUP Gene;
=Gene or Genome | - 267. Juvenile Type Ovarian Granulosa Cell Tumor
- (UMLS (NCI) C1334304) =Neoplastic Process
|
- 230. Junctional Proliferation
- (UMLS (NCI) C1334302) =Finding
| - 268. Juvenile Xanthogranuloma
- [A benign fibrohistiocytic lesion that occurs during childhood; it is distinct from Langerhans cell histiocytosis. The lesions usually develop during infancy, and are characterized by regressing cutaneous nodules (most often in the head and neck) sometimes associated with deep soft tissues nodules. The prognosis is excellent. — 2003 ( NCI )] (UMLS (NCI) C0043324) =Neoplastic Process =Histiocytosis, Non-Langerhans-Cell;
Skin Diseases, Metabolic |
- 231. Junctional Tachycardia
- [A rare form of supraventricular tachycardia caused by automatic, not reentrant, conduction initiated from sites at the atrioventricular junction, but not the ATRIOVENTRICULAR NODE. It usually occurs during myocardial infarction, after heart surgery, or in digitalis intoxication with a HEART RATE ranging from 140 to 250 beats per minute. ( MSH )] (UMLS (NCI) C0039235) =Disease or Syndrome =Supraventricular Tachycardia;
| - 269. Juxtaarticular Myxoma
- [A cellular myxoma arising from the joints. ( NCI )] (UMLS (NCI) C1334305) Juxta-Articular Myxoma =Neoplastic Process
|
- 232. Junin virus
- [Junin virus vaccine ( HL7V3.0 )] (UMLS (HL7) C1548482) =Pharmacologic Substance; Immunologic Factor ;
=Vaccines administered (code = CVX)(parenteral, unless oral is noted);
VaccineType | - 270. Juxtacortical Chondroma
- [A benign neoplasm composed of hyaline cartilage arising from the periosteum of the bone. It is characterized by the presence of chondrocytes, a lobulated growth pattern, and calcification. ( NCI )] (UMLS (NCI) C0334548) =Neoplastic Process
|
- 233. junk DNA
- [ ] (UMLS (CSP) C0599904) =Nucleic Acid, Nucleoside, or Nucleotide ;
| - 271. Juxtacortical Chondrosarcoma
- [A chondrosarcoma arising from the surface of bone. It is characterized by a lobulated growth pattern, high mitotic activity, myxoid stroma formation, and necrotic changes. It occurs in adults. Clinical presentation includes pain, and sometimes swelling. ( NCI )] (UMLS (NCI) C0334549) =Neoplastic Process
|
- 234. Juris Doctor
- (UMLS (HL7) C1549972) =Intellectual Product =Degree/license/certificate;
| - 272. Juxtacortical Osteogenic Sarcoma
- [A low grade malignant bone-forming mesenchymal neoplasm arising from the surface of the bone. It usually affects the distal posterior femur, the proximal tibia, and proximal humerus. Painless swelling is the usual clinical sign. Most patients are young adults and the prognosis is usually excellent. ( NCI )] (UMLS (NCI) C0206642) =Neoplastic Process =Osteogenic Sarcoma;
|
- 235. Jurisdictional Breadth
- (UMLS (HL7) C1547917) =Spatial Concept =HL7 Vocabulary Version 2.5;
=County/Parish;
State/Province;
Country | - 273. juxtaglomerular apparatus
- [specialized cells containing secretory granules, located in the tunica media of the afferent glomerular arterioles; major structural component responsible for the release of renin; play a major role in renal autoregulation. ( CSP )] (UMLS (CSP) C0022445) =Body Part, Organ, or Organ Component =kidney;
|
- 236. Jurisdictional health number (Canada)
- (UMLS (HL7) C1549706) =Idea or Concept =Identifier type;
| - 274. Juxtaglomerular Cell
- [Any of a group of cells that are situated in the wall of each afferent arteriole of a kidney glomerulus near its point of entry adjacent to a macula densa and that produce and secrete renin. ( NCI )] (UMLS (NCI) C0227650) =Cell
|
- 237. jurisprudence
- [The science or philosophy of law. Also, the application of the principles of law and justice to health and medicine. ( MSH )] (UMLS (CSP) C0022433) =Governmental or Regulatory Activity
| - 275. juxtaglomerular cell hyperplasia
- [ ] (UMLS (CSP) C0597966) =Congenital Abnormality; Disease or Syndrome
|
- 238. Jurkat cell
- [A CELL LINE derived from human T-CELL LEUKEMIA and used to determine the mechanism of differential susceptibility to anti-cancer drugs and radiation. ( MSH )] (UMLS (CSP) C0376448) =Cell
| - 276. Juxtaglomerular Cell Tumor
- [A benign, well circumscribed neoplasm arising from the cortex of the kidney. It secrets renin and the patients usually present with severe hypertension and marked hypokalemia. Morphologically, it is characterized by the presence of sheets of polygonal or spindle-shaped neoplastic cells forming a hemangiopericytic pattern. ( NCI )] (UMLS (NCI) C0334331) =Neoplastic Process
|
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