Neoplastic Syndromes, Hereditary [dědičné nádorové syndromy]

topical
144
Terms

hereditární malignity
hereditární nádorová onemocnění
hereditární nádorové syndromy
nádorové syndromy dědičné

 

Cancer Syndromes, Hereditary
Hereditary Cancer Syndromes
Hereditary Neoplastic Syndromes

Persistent link   https://www.medvik.cz/link/D009386
Definition

The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance.

Annotation
coordinate with specific hereditary organ/neoplasm term or specific hereditary histological type
DUI
D009386 MeSH Browser
CUI
M0014613
History note
87
Public note
87

C Diseases
C04 Neoplasms 12 832
C04.182 Cysts 723
C04.445 Hamartoma 128
C04.700.600 Li-Fraumeni Syndrome 39
C04.700.631 Neurofibromatoses 28
C04.700.700 Tuberous Sclerosis 144
C04.700.900 Wilms Tumor 112
C16.320.051 Alagille Syndrome 19
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.365 Hemoglobinopathies 68
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.540 Marfan Syndrome 105
C16.320.577 Muscular Dystrophies 141
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
C16.320.728 Osteochondrodysplasias 125
C16.320.784 Pelger-Huet Anomaly 7
C16.320.812 Pycnodysostosis 2
C16.320.925 Werner Syndrome 14

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