serw-MX  [xml]  
 


    
 DeCS Categories

B01 Eukaryota .
B01.650 Plants .
B01.650.940 Viridiplantae .
B01.650.940.800 Streptophyta .
B01.650.940.800.575 Embryophyta .
B01.650.940.800.575.912 Tracheophyta .
B01.650.940.800.575.912.250 Magnoliopsida .
B01.650.940.800.575.912.250.475 Hamamelidaceae .
B01.650.940.800.575.912.250.475.500 Hamamelis .
C04 Neoplasms .
C04.445 Hamartoma .
C04.445.435 Hamartoma Syndrome, Multiple .
C04.651 Neoplasms, Multiple Primary .
C04.651.435 Hamartoma Syndrome, Multiple .
C04.700 Neoplastic Syndromes, Hereditary .
C04.700.435 Hamartoma Syndrome, Multiple .
C04.700.705 Peutz-Jeghers Syndrome .
C06 Digestive System Diseases .
C06.405 Gastrointestinal Diseases .
C06.405.469 Intestinal Diseases .
C06.405.469.578 Intestinal Polyposis .
C06.405.469.578.750 Peutz-Jeghers Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.700 Neoplastic Syndromes, Hereditary .
C16.320.700.435 Hamartoma Syndrome, Multiple .
C16.320.700.705 Peutz-Jeghers Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.621 Pigmentation Disorders .
C17.800.621.430 Hyperpigmentation .
C17.800.621.430.530 Melanosis .
C17.800.621.430.530.550 Lentigo .
C17.800.621.430.530.550.625 Peutz-Jeghers Syndrome .
D03 Heterocyclic Compounds .
D03.633 Heterocyclic Compounds, Fused-Ring .
D03.633.100 Heterocyclic Compounds, 2-Ring .
D03.633.100.759 Purines .
D03.633.100.759.160 Allopurinol .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Hamartoma .
Hamartomas .
A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. .
1.00
2896787
 
Allopurinol .
Allohexal .
Allohexan .
Alloprin .
Allopurin .
Allorin .
Allpargin .
Allural .
Apulonga .
Apurin .
Atisuril .
Bleminol .
Caplenal .
Capurate .
Cellidrin .
Embarin .
Foligan .
Hamarin .
Jenapurinol .
Lopurin .
Lysuron .
Milurit .
Milurite .
Novopurol .
Pan Quimica .
Progout .
Pureduct .
Purinol .
Remid .
Rimapurinol .
Roucol .
Suspendol .
Tipuric .
Uribenz .
Uridocid .
Uripurinol .
Urosin .
Urtias .
Xanthomax .
Xanturic .
Zygout .
Zyloprim .
Zyloric .
A XANTHINE OXIDASE inhibitor that decreases URIC ACID production. It also acts as an antimetabolite on some simpler organisms. .
0.75
1167096
 
Hamartoma Syndrome, Multiple .
Bannayan-Ruvalcaba-Riley Syndrome .
Bannayan-Zonana Syndrome .
Cowden Syndrome .
Cowden's Syndrome .
Dysplastic Gangliocytoma of Cerebellum .
Dysplastic Gangliocytoma of the Cerebellum .
Macrocephaly, Multiple Lipomas, and Hemangiomata .
Macrocephaly, Pseudopapilledema, and Multiple Hemangiomas .
Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata .
Myhre-Riley-Smith Syndrome .
Riley-Smith Syndrome .
Ruvalcaba-Myhre Syndrome .
Ruvalcaba-Myhre-Smith Syndrome .
Bannayan Riley Ruvalcaba Syndrome .
Bannayan Zonana Syndrome .
Cerebellum Dysplastic Gangliocytoma .
Cerebellum Dysplastic Gangliocytomas .
Cowdens Disease .
Cowdens Syndrome .
Hamartoma Syndromes, Multiple .
Lhermitte Duclos Disease .
Multiple Hamartoma Syndromes .
Myhre Riley Smith Syndrome .
Riley Smith Syndrome .
Ruvalcaba Myhre Smith Syndrome .
Bannayan-Riley-Ruvalcaba Syndrome .
Cowden Disease .
Cowden's Disease .
Lhermitte-Duclos Disease .
Multiple Hamartoma Syndrome .
PTEN Hamartoma Tumor Syndrome .
A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE. .
0.63
34930
 
Hamamelis .
Hamamelis virginiana .
Hamameli .
Hamamelis virginianas .
Hazel, Witch .
Hazels, Witch .
Witch Hazels .
virginianas, Hamamelis .
Witch Hazel .
A plant genus of the family Hamamelidaceae, order Hamamelidales. It is known for the astringent (ASTRINGENTS) extract of leaves and bark used in over the counter preparations. This should not be confused with the similar named Hamelia genus (RUBIACEAE). .
0.61
330
 
Peutz-Jeghers Syndrome .
Periorificial Lentiginosis Syndrome .
Peutz-Jegher's Syndrome .
Peutz-Jeghers Polyposis .
Polyposis, Hamartomatous Intestinal .
Polyps-and-Spots Syndrome .
Hamartomatous Intestinal Polyposes .
Hamartomatous Intestinal Polyposis .
Intestinal Polyposes, Hamartomatous .
Intestinal Polyposis, Hamartomatous .
Lentiginoses, Perioral .
Perioral Lentiginoses .
Perioral Lentiginosis .
Periorificial Lentiginosis Syndromes .
Peutz Jegher's Syndrome .
Peutz Jeghers Polyposis .
Peutz Jeghers Syndrome .
Peutz-Jegher Syndrome .
Polyposes, Hamartomatous Intestinal .
Polyposis, Peutz-Jeghers .
Polyps and Spots Syndrome .
Polyps-and-Spots Syndromes .
Syndrome, Periorificial Lentiginosis .
Syndrome, Peutz-Jegher's .
Syndrome, Peutz-Jeghers .
Syndrome, Polyps-and-Spots .
Syndromes, Periorificial Lentiginosis .
Syndromes, Polyps-and-Spots .
Lentiginosis, Perioral .
A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. .
0.58