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Term:
Parent Terms Term With Siblings Child Terms
inherited disease susceptibility +   
A latent susceptibility to disease at the genetic level, which may be activated under certain conditions.
 accelerated tumor formation, susceptibility to 
 age related macular degeneration, susceptibility to +  
 amyotrophic lateral sclerosis, susceptibility to, 13 
 amyotrophic lateral sclerosis, susceptibility to, 24 
 aplastic anemia, susceptibility to 
 Asperger syndrome, susceptibility to 
 aspergillosis, susceptibility to 
 atrioventricular septal defect, susceptibility to, 2 
 autism, susceptiblity to +  
 autoimmune thyroid disease, susceptibility to 
 autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency 
 autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency 
 bacteremia, susceptibility +  
 basal cell carcinoma, susceptibility to +  
 bleeding diathesis due to thromboxane synthesis deficiency 
 bleeding disorder, platelet-type, 13, susceptibility to 
 breast-ovarian cancer, familial, susceptibility to +  
 cardiomyopathy, familial hypertrophic, 4, susceptibility to 
 celiac disease, susceptibility to, 3 
 cirrhosis, noncryptogenic, susceptibility to 
 coronary artery disease, severe, susceptibility to 
 coronary heart disease, susceptibility to, 1 
 coronary heart disease, susceptibility to, 2 
 coronary heart disease, susceptibility to, 7 
 craniosynostosis 5, susceptibility to 
 craniosynostosis 7 
 dengue virus, susceptibility to 
 dermatitis, atopic, susceptibility to +  
 diabetes mellitus, insulin-dependent, X-linked, susceptibility to +  
 encephalitis, acute, infection-induced, susceptibility to +  
 epilepsy, childhood absence, susceptibility to, 5 
 epilepsy, idiopathic generalized, susceptibility to, 17 
 epilepsy, idiopathic generalized, susceptibility to, 18 
 epilepsy, idiopathic generalized, susceptibility to, 6 
 epilepsy, idiopathic generalized, susceptibility to, 8 
 epilepsy, idiopathic generalized, susceptibility to, 9 
 epilepsy, juvenile absence, susceptibility to +  
 epilepsy, juvenile myoclonic, susceptibility to, 6 
 essential hypertension, genetic 
 exfoliation syndrome, susceptibility to 
 familial meningioma 
 GBA1-related Parkinson disease, susceptibility 
 graft-versus-host disease, susceptibility to 
 hearing loss, noise-induced, susceptibility to 
 Helicobacter pylori infection, susceptibility to 
 hemolytic uremic syndrome, atypical, susceptibility to, 1 +  
 hepatitis B virus, susceptibility to 
 hepatitis C virus, susceptibility to 
 hepatitis, fulminant viral, susceptibility to 
 hereditary neoplastic syndrome +   
 herpes simplex encephalitis, susceptibility to, 3 
 herpes simplex encephalitis, susceptibility to, 4 
 Hirschsprung disease, susceptibility to +  
 hydrocephalus, congenital, 5, susceptibility to 
 hyperemesis gravidarum, susceptibility to 
 IgA nephropathy, susceptibility to 
 influenza, severe, susceptibility to 
 inherited susceptibility to asthma +  
 inherited susceptibility to mycobacterial diseases +  
 iron overload, susceptibility to 
 kuru, susceptibility to 
 legionnaire disease, susceptibility to 
 lipodystrophy, partial, acquired, susceptibility to 
 lumbar disk degeneration, susceptibility to 
 lumbar disk herniation, susceptibility to 
 malaria, susceptibility to +  
 malignant hyperthermia, susceptibility to +  
 microvascular complications of diabetes, susceptibility +  
 migraine with or without aura, susceptibility to +   
 multiple sclerosis, susceptibility to +  
 multiple system atrophy 1, susceptibility to 
 Mycobacterium tuberculosis, susceptibility +  
 myoclonic epilepsy, juvenile, susceptibility to, 1 
 nephrolithiasis susceptibility caused by SLC26A1 
 neural tube defects, susceptibility to 
 opioid dependence, susceptibility to, 1 
 orofacial cleft 6, susceptibility to 
 osteoarthritis susceptibility 2 
 osteoarthritis susceptibility 5 
 otitis media, susceptibility to 
 Parkinson disease 13, autosomal dominant, susceptibility to 
 Parkinson disease 24, autosomal dominant, susceptibility to 
 Parkinson disease 5, autosomal dominant, susceptibility to 
 polysubstance abuse, susceptibility to 
 predisposition to invasive fungal disease due to CARD9 deficiency 
 psoriatic arthritis, susceptibility to 
 pulmonary disease, chronic obstructive, susceptibility to 
 rhabdomyolysis, susceptibility to, 1 
 schizophrenia, susceptibility to +  
 scoliosis, isolated, susceptibility to, 1 
 sick sinus syndrome 3, susceptibility to 
 spondyloarthropathy, susceptibility to +  
 strabismus, susceptibility to 
 susceptibility to HIV infection 
 susceptibility to mononeuropathy of the median nerve, mild 
 susceptibility to respiratory infections associated with CD8alpha chain mutation 
 susceptibility to severe covid-19 
 systemic lupus erythematosus, susceptibility to, 1 
 systemic lupus erythematosus, susceptibility to, 11 
 systemic lupus erythematosus, susceptibility to, 9 
 thyrotoxic periodic paralysis, susceptibility to, 1 
 UV-induced skin damage, susceptibility to 
 vitiligo-associated multiple autoimmune disease susceptibility 1 
 West Nile virus, susceptibility to 

Synonyms
Exact Synonyms: hereditary disease susceptibility ;   hereditary predisposition to disease
Related Synonyms: genetic predisposition ;   genetic predispositions ;   genetic susceptibilities ;   genetic susceptibility
Alternate IDs: MONDO:0020573
Xrefs: ICD10CM:Z15 ;   MEDGEN:137259 ;   MESH:D020022 ;   UMLS:C0314657
Definition Sources: MESH:D020022

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