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Disease association ontology term - MONDO:0020573 - inherited disease susceptibility

Term summary

ID
MONDO:0020573
Name
inherited disease susceptibility
Ontology or CV name
Disease association
Definition
A latent susceptibility to disease at the genetic level, which may be activated under certain conditions.

Parents

Annotation

Disease association

MONDO:0013409 - age related macular degeneration 5

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MONDO:0859575 - Atelis syndrome 1

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MONDO:0859576 - Atelis syndrome 2

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MONDO:0700270 - ATM-related cancer predisposition

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MONDO:0013258 - autism, susceptibility to, 16

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MONDO:0014041 - autism, susceptibility to, 19

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MONDO:0010449 - autism, susceptibility to, X-linked 5

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MONDO:0027353 - autosomal recessive dyskeratosis congenita 4

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MONDO:0013253 - breast-ovarian cancer, familial, susceptibility to, 3

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MONDO:0013669 - breast-ovarian cancer, familial, susceptibility to, 4

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MONDO:0012499 - Buruli ulcer, susceptibility to

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MONDO:0011740 - Carney-Stratakis syndrome

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MONDO:0021055 - classic familial adenomatous polyposis

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MONDO:0012953 - colorectal cancer, susceptibility to, 10

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MONDO:0014038 - colorectal cancer, susceptibility to, 12

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MONDO:0015780 - dyskeratosis congenita

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MONDO:0007485 - dyskeratosis congenita, autosomal dominant 1

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MONDO:0013521 - dyskeratosis congenita, autosomal dominant 2

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MONDO:0013522 - dyskeratosis congenita, autosomal dominant 3

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MONDO:0014690 - dyskeratosis congenita, autosomal dominant 6

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MONDO:0009136 - dyskeratosis congenita, autosomal recessive 1

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MONDO:0013519 - dyskeratosis congenita, autosomal recessive 2

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MONDO:0013520 - dyskeratosis congenita, autosomal recessive 3

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MONDO:0014600 - dyskeratosis congenita, autosomal recessive 6

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MONDO:0031057 - dyskeratosis congenita, digenic

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MONDO:0010584 - dyskeratosis congenita, X-linked

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MONDO:0980989 - dystonia 38, susceptibility to

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MONDO:0030334 - encephalitis, acute, infection (viral)-induced, susceptibility to, 11

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MONDO:0032742 - encephalopathy, acute, infection-induced, susceptibility to, 9

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MONDO:0060671 - epilepsy, juvenile myoclonic, susceptibility to, 10

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MONDO:0007781 - essential hypertension, genetic

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MONDO:0012041 - familial adenomatous polyposis 2

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MONDO:0014630 - familial adenomatous polyposis 3

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MONDO:0044300 - familial adenomatous polyposis 4

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MONDO:0013806 - familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome

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MONDO:0011789 - familial meningioma

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MONDO:1010151 - gallbladder disease 4

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MONDO:0011693 - glaucoma, normal tension, susceptibility to

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MONDO:0024498 - glioma susceptibility 1

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MONDO:0013092 - glioma susceptibility 2

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MONDO:0007681 - goiter, multinodular 1, with or without Sertoli-Leydig cell tumors

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MONDO:0007888 - hereditary leiomyomatosis and renal cell cancer

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MONDO:0018630 - hereditary nonpolyposis colon cancer

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MONDO:0859376 - hydrocephalus, congenital, 5, susceptibility to

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MONDO:0007767 - hyperparathyroidism 1

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MONDO:0007768 - hyperparathyroidism 2 with jaw tumors

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MONDO:0013108 - leukemia, acute lymphocytic, susceptibility to, 1

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MONDO:0018875 - Li-Fraumeni syndrome

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MONDO:0005835 - Lynch syndrome

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MONDO:0007356 - Lynch syndrome 1

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MONDO:0012249 - Lynch syndrome 2

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MONDO:0013699 - Lynch syndrome 4

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MONDO:0013710 - Lynch syndrome 5

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MONDO:0021024 - malaria, susceptibility to

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MONDO:0013510 - melanoma, cutaneous malignant, susceptibility to, 6

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MONDO:0014056 - melanoma, cutaneous malignant, susceptibility to, 9

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MONDO:0012970 - microvascular complications of diabetes, susceptibility to, 6

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MONDO:0010159 - mismatch repair cancer syndrome 1

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MONDO:0009759 - mosaic variegated aneuploidy syndrome 1

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MONDO:0013582 - mosaic variegated aneuploidy syndrome 2

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MONDO:0859346 - mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition

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MONDO:0008018 - Muir-Torre syndrome

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MONDO:0020715 - multiple system atrophy 1, susceptibility to

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MONDO:0000070 - Mycobacterium tuberculosis, susceptibility

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MONDO:0012039 - myocardial infarction, susceptibility to

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MONDO:0010686 - N syndrome

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MONDO:0020722 - nephrolithiasis susceptibility caused by SLC26A1

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MONDO:0011896 - Parkinson disease 11, autosomal dominant, susceptibility to

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MONDO:0012466 - Parkinson disease 13, autosomal dominant, susceptibility to

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MONDO:0008192 - pheochromocytoma/paraganglioma syndrome 1

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MONDO:0011121 - pheochromocytoma/paraganglioma syndrome 2

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MONDO:0011544 - pheochromocytoma/paraganglioma syndrome 3

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MONDO:0007273 - pheochromocytoma/paraganglioma syndrome 4

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MONDO:0013602 - pheochromocytoma/paraganglioma syndrome 5

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MONDO:0032771 - pheochromocytoma/paraganglioma syndrome 7

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MONDO:0011685 - polysubstance abuse, susceptibility to

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MONDO:0008318 - Proteus syndrome

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MONDO:0014494 - psoriasis 15, pustular, susceptibility to

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MONDO:0017623 - PTEN hamartoma tumor syndrome

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MONDO:0011037 - renal dysplasia, cystic, susceptibility to

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MONDO:0009990 - Revesz syndrome

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MONDO:0012252 - rhabdoid tumor predisposition syndrome 1

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MONDO:0013224 - rhabdoid tumor predisposition syndrome 2

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MONDO:0980721 - rhabdomyolysis, susceptibility to, 2

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MONDO:0010002 - Rothmund-Thomson syndrome

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MONDO:0016368 - Rothmund-Thomson syndrome type 1

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MONDO:0016369 - Rothmund-Thomson syndrome type 2

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MONDO:0970950 - Rothmund-Thomson syndrome type 4

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MONDO:0010943 - schizophrenia 4

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MONDO:0013568 - sick sinus syndrome 3, susceptibility to

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MONDO:0024517 - SMARCB1-related schwannomatosis

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MONDO:0100003 - susceptibility to angioedema induced by ACE inhibitors

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MONDO:0001734 - tuberous sclerosis

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MONDO:0008612 - tuberous sclerosis 1

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MONDO:0013199 - tuberous sclerosis 2

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MONDO:0014368 - tumor predisposition syndrome 3

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MONDO:0010863 - type 1 diabetes mellitus 5

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MONDO:0010518 - Wiskott-Aldrich syndrome

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MONDO:0010389 - X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency

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