Hamartoma Syndrome, Multiple [syndrom mnohočetného hamartomu]

topical
25
Terms

Bannayanův Zonanaův syndrom
Cowdenova nemoc
Cowdenův syndrom
dysplastický gangliocytom mozečku
makrocefalie, mnohočetné lipomy a hemangiomy
PTEN hamartoma syndrom

 

Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Ruvalcaba-Riley Syndrome
Bannayan-Zonana Syndrome
Cowden Disease
Cowden Syndrome
Cowden's Disease
Cowden's Syndrome
Dysplastic Gangliocytoma of Cerebellum
Dysplastic Gangliocytoma of the Cerebellum
Lhermitte-Duclos Disease
Macrocephaly, Multiple Lipomas, and Hemangiomata
Macrocephaly, Pseudopapilledema, and Multiple Hemangiomas
Macrocephaly, Pseudopapilledema, and Multiple Hemangiomata
Multiple Hamartoma Syndrome
Myhre-Riley-Smith Syndrome
PTEN Hamartoma Tumor Syndrome
Riley-Smith Syndrome
Ruvalcaba-Myhre Syndrome
Ruvalcaba-Myhre-Smith Syndrome

Persistent link   https://www.medvik.cz/link/D006223
Definition

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.

DUI
D006223 MeSH Browser
CUI
M0009775
Previous indexing
Hamartoma (1966-1986); Neoplasms, Multiple Primary (1966-1986)
History note
91(87); was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90
Public note
91; was see under NEOPLASMS, MULTIPLE PRIMARY 1987-90

Allowable subheadings

BL
blood 0
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 1
CO
complications 2
CN
congenital 1
DI
diagnosis 13
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 0
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 1
EH
ethnology 0
ET
etiology 4
GE
genetics 13
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 0
NU
nursing 0
PS
parasitology 0
PA
pathology 5
PP
physiopathology 0
PC
prevention & control 2
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 0
SU
surgery 1
TH
therapy 2
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C04 Neoplasms 12 762
C04.445 Hamartoma 127
C04.445.435 Hamartoma Syndrome, Multiple 25
C04.445.435.500 Proteus Syndrome 8
C04.445.622 Pallister-Hall Syndrome
C04.445.810 Tuberous Sclerosis 141
C04.651 Neoplasms, Multiple Primary 157
C04.651.435 Hamartoma Syndrome, Multiple 25
C04.651.435.500 Proteus Syndrome 8
C04.651.600 Multiple Endocrine Neoplasia 32
C04.651.800 Tuberous Sclerosis 141
C04.700 Neoplastic Syndromes, Hereditary 143
C04.700.100 Adenomatous Polyposis Coli 92
C04.700.175 Basal Cell Nevus Syndrome 32
C04.700.212 Birt-Hogg-Dube Syndrome 8
C04.700.250 Colorectal Neoplasms, Hereditary Nonpolyposis 114
C04.700.305 Dysplastic Nevus Syndrome 17
C04.700.330 Exostoses, Multiple Hereditary 12
C04.700.435 Hamartoma Syndrome, Multiple 25
C04.700.517 Hereditary Breast and Ovarian Cancer Syndrome 53
C04.700.600 Li-Fraumeni Syndrome 39
C04.700.630 Multiple Endocrine Neoplasia 32
C04.700.631 Neurofibromatoses 28
C04.700.633 Peutz-Jeghers Syndrome 37
C04.700.700 Tuberous Sclerosis 141
C04.700.900 Wilms Tumor 112
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.700 Neoplastic Syndromes, Hereditary 143
C16.320.700.100 Adenomatous Polyposis Coli 92
C16.320.700.175 Basal Cell Nevus Syndrome 32
C16.320.700.212 Birt-Hogg-Dube Syndrome 8
C16.320.700.250 Colorectal Neoplasms, Hereditary Nonpolyposis 114
C16.320.700.305 Dysplastic Nevus Syndrome 17
C16.320.700.330 Exostoses, Multiple Hereditary 12
C16.320.700.435 Hamartoma Syndrome, Multiple 25
C16.320.700.517 Hereditary Breast and Ovarian Cancer Syndrome 53
C16.320.700.600 Li-Fraumeni Syndrome 39
C16.320.700.630 Multiple Endocrine Neoplasia 32
C16.320.700.633 Neurofibromatoses 28
C16.320.700.667 Peutz-Jeghers Syndrome 37
C16.320.700.700 Tuberous Sclerosis 141
C16.320.700.900 Wilms Tumor 112

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