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

C Diseases
C04 Neoplasms 12 832
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
C04.700.600 Li-Fraumeni Syndrome 39
C04.700.631 Neurofibromatoses 28
C04.700.700 Tuberous Sclerosis 144
C04.700.900 Wilms Tumor 112
C05.116 Bone Diseases 796
C05.116.099.708 Osteochondrodysplasias 125
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 22
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
C16.320.700.100 Adenomatous Polyposis Coli 93
C16.320.700.175 Basal Cell Nevus Syndrome 33
C16.320.700.212 Birt-Hogg-Dube Syndrome 8
C16.320.700.305 Dysplastic Nevus Syndrome 17
C16.320.700.600 Li-Fraumeni Syndrome 39
C16.320.700.633 Neurofibromatoses 28
C16.320.700.667 Peutz-Jeghers Syndrome 37
C16.320.700.700 Tuberous Sclerosis 144
C16.320.700.900 Wilms Tumor 112

Chondrodysplasia, blomstrand type Disease MeSH Browser

Dermochondrocorneal dystrophy of François Disease MeSH Browser

Dysplasia Epiphysealis Hemimelica with Chondromas and Osteochondromas Disease MeSH Browser

Exostoses Of Heel Disease MeSH Browser

Exostoses, Multiple, Type III Disease MeSH Browser

Kniest like dysplasia lethal Disease MeSH Browser

Metachondromatosis Disease MeSH Browser

Metaphyseal acroscyphodysplasia Disease MeSH Browser

Multiple Exostoses with Spastic Tetraparesis Disease MeSH Browser

Polyposis, Intestinal, With Multiple Exostoses Disease MeSH Browser

Potocki-Shaffer syndrome Disease MeSH Browser

Stuve-Wiedemann syndrome Disease MeSH Browser