- 1. 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 ;
| - 15. juvenile delinquency
- [antisocial behavior by youths which is subject to legal sanctions. ( CSP )] (UMLS (CSP) C0022438) =Individual Behavior =child behavior disorder;
social disturbance |
- 2. JUV OSTEOCHONDROS PELVIS
- (UMLS (ICD9CM) C0022441) =Disease or Syndrome
| - 16. juvenile hormone
- [natural or synthetic compounds which prevent metamorphosis in the growing insect. ( CSP )] (UMLS (CSP) C0022439) =Hormone =Fatty Acids, Unsaturated;
invertebrate hormone |
- 3. JUV OSTEOCHONDROS SPINE
- [Osteochondrosis of the vertebral epiphyses in children. ( MSH )] (UMLS (ICD9CM) C0036310) =Disease or Syndrome =osteochondritis;
DORSOPATHIES | - 17. Juvenile Multiple Polyps Syndrome
- (UMLS (NCI) C0345893) =Neoplastic Process
|
- 4. JUV OSTEOCHONDROSIS ARM
- [ ] (UMLS (ICD9CM) C0158442) =Disease or Syndrome
| - 18. 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;
|
- 5. JUV OSTEOCHONDROSIS FOOT
- [ ] (UMLS (ICD9CM) C0158444) =Disease or Syndrome
| - 19. JUVENILE NEUROSYPH NEC
- [ ] (UMLS (ICD9CM) C0153135) =Disease or Syndrome
|
- 6. JUV OSTEOCHONDROSIS LEG
- [ ] (UMLS (ICD9CM) C1282912) Juvenile osteochondrosis of lower extremity, excluding foot;
=Disease or Syndrome | - 20. JUVENILE NEUROSYPH NOS
- [ ] (UMLS (ICD9CM) C0153132) =Disease or Syndrome
|
- 7. JUV OSTEOCHONDROSIS NEC
- [ ] (UMLS (ICD9CM) C0158445) =Disease or Syndrome
| - 21. Juvenile Osteochondrosis
- (UMLS (NCI) C0729346) =Disease or Syndrome ;
|
- 8. JUV RHEUM ARTHRITIS NOS
- [ ] (UMLS (ICD9CM) C0837691) Polyarticular juvenile rheumatoid arthritis, chronic or unspecified =Disease or Syndrome
| - 22. 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;
|
- 9. 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 ;
| - 23. Juvenile Pilocytic Astrocytoma
- (UMLS (NCI) C0280783) =Neoplastic Process
|
- 10. JUVEN DERMAT HERPETIFORM
- [ ] (UMLS (ICD9CM) C0152092) =Disease or Syndrome
| - 24. Juvenile Polyp
- (UMLS (NCI) C0221273) =Neoplastic Process ;
|
- 11. juvenile animal
- [animal between infancy and adulthood. ( CSP )] (UMLS (CSP) C0598744) =Animal ;
=immature animal;
| - 25. Juvenile Polyp of Rectum
- (UMLS (NCI) C1335680) Juvenile Polyp of the Rectum;
Rectal Juvenile Polyp =Disease or Syndrome ;
|
- 12. Juvenile Breast Papillomatosis
- (UMLS (NCI) C1334303) Juvenile Papillomatosis of Breast;
Juvenile Papillomatosis of the Breast;
=Neoplastic Process | - 26. 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
|
- 13. Juvenile Cataract
- (UMLS (NCI) C0302254) =Anatomical Abnormality
| - 27. Juvenile Type Ovarian Granulosa Cell Tumor
- (UMLS (NCI) C1334304) =Neoplastic Process
|
- 14. Juvenile chronic polyarthritis
- [ ] (UMLS (ICD9CM) C0409667) =Disease or Syndrome
| - 28. 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 |
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