Exostoses, Multiple Hereditary [dědičné mnohočetné exostózy]

topical
12
Terms

exostózy mnohočetné
exostózy mnohočetné dědičné
mnohočetná hereditární osteochondromatóza
syndrom mnohočetných osteokartilaginozních exostóz
vrozené mnohočetné exostózy

 

Bessel-Hagen Disease
Chondrodysplasia, Hereditary Deforming
Diaphyseal Aclasis
Exostoses, Familial
Exostoses, Hereditary Multiple
Exostoses, Multiple
Exostoses, Multiple Cartilaginous
Exostoses, Multiple, Type I
Exostosis, Familial
Exostosis, Hereditary Multiple
Exostosis, Multiple
Exostosis, Multiple Cartilaginous
Familial Exostoses
Hereditary Multiple Exostoses
Hereditary Multiple Exostosis
Multiple Cartilaginous Exostoses
Multiple Hereditary Exostoses
Multiple Osteochondromas
Multiple Osteochondromatosis
Osteochondromas, Multiple

Persistent link   https://www.medvik.cz/link/D005097
Definition

Hereditary disorder transmitted by an autosomal dominant gene and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation.

DUI
D005097 MeSH Browser
CUI
M0008037
Previous indexing
Exostoses (1966-1967)
History note
90; was EXOSTOSES, MULTIPLE 1968-89
Online note
use EXOSTOSES, MULTIPLE HEREDITARY to search EXOSTOSES, MULTIPLE 1968-89
Public note
90; was EXOSTOSES, MULTIPLE 1968-89

Allowable subheadings

BL
blood 0
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 0
CO
complications 2
CN
congenital 1
DI
diagnosis 3
DG
diagnostic imaging 3
DH
diet therapy 0
DT
drug therapy 0
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 0
EH
ethnology 0
ET
etiology 1
GE
genetics 4
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 0
NU
nursing 0
PS
parasitology 0
PA
pathology 2
PP
physiopathology 0
PC
prevention & control 0
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 0
SU
surgery 2
TH
therapy 1
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C04 Neoplasms 12 762
C04.557 Neoplasms by Histologic Type 270
C04.557.450 Neoplasms, Connective and Soft Tissue 45
C04.557.450.565 Neoplasms, Connective Tissue 122
C04.557.450.565.575 Neoplasms, Bone Tissue 29
C04.557.450.565.575.610 Osteochondroma 16
C04.557.450.565.575.610.615 Osteochondromatosis 10
C04.557.450.565.575.610.615.325 Exostoses, Multiple Hereditary 12
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
C05 Musculoskeletal Diseases 1 119
C05.116 Bone Diseases 792
C05.116.099 Bone Diseases, Developmental 291
C05.116.099.708 Osteochondrodysplasias 123
C05.116.099.708.670 Osteochondroma 16
C05.116.099.708.670.615 Osteochondromatosis 10
C05.116.099.708.670.615.325 Exostoses, Multiple Hereditary 12
C05.116.540 Hyperostosis 21
C05.116.540.310 Exostoses 49
C05.116.540.310.500 Exostoses, Multiple Hereditary 12
C05.116.540.310.600 Heel Spur 28
C05.116.540.310.800 Osteophyte 3
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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