Related by context. All words. (Click for frequent words.) 65 hereditary predisposition 63 inherited predisposition 62 Genetic mutation 62 ADPKD 62 precancerous condition 62 Hashimoto thyroiditis 62 spontaneous remission 62 familial adenomatous polyposis 62 underactive thyroid gland 61 untreated celiac disease 61 familial ALS 61 cryptogenic 61 polymorphic ventricular tachycardia 60 Genetic mutations 60 inherited mutations 60 fronto temporal dementia 60 testicular tumors 60 nonmelanoma skin cancers 59 Sporadic CJD 59 familial hypercholesterolemia 59 xeroderma pigmentosum 59 breast endometrial 59 Epstein Barr virus EBV 59 Raynaud disease 59 TP# mutation 59 herpes zoster virus 59 Cryptococcus neoformans 59 Von Hippel Lindau 59 Chronic pancreatitis 59 progressive multifocal PML 59 eosinophilic esophagitis 59 GBA mutations 59 lichen planus 58 dyskeratosis congenita 58 Myocarditis 58 underactive thyroid 58 G6PD deficiency 58 KRAS oncogene 58 Hyperthyroidism 58 hepatitis B infection 58 BRAF gene 58 Dravet syndrome 58 biochemical imbalance 58 HNPCC 58 myopathies 58 orchitis 58 polycystic kidneys 58 alveolar rhabdomyosarcoma 58 Coeliac disease 58 Cholangiocarcinoma 58 PCNSL 58 liver scarring 57 progranulin mutations 57 Medulloblastoma 57 gene APOE4 57 familial polyposis 57 Male pattern baldness 57 DFMO 57 mitochondrial mutations 57 aneuploidies 57 carcinoid tumor 57 genetic defect 57 Leukemias 57 de novo mutations 57 narcolepsy cataplexy 57 achromatopsia 57 herpesviruses 57 LQTS 57 gonococcal 57 squamous cell lung cancer 57 HLA B# 57 congenital blindness 57 mutated K ras 57 Beta thalassemia 57 microvascular angina 57 PARP inhibition 57 Melasma 57 Carcinoid tumors 57 enteroviruses 56 IgA deficiency 56 thyroid deficiency 56 abnormal Pap smear 56 chromosome abnormality 56 familial pancreatic cancer 56 chronic granulomatous disease 56 cystic fibrosis chronic pancreatitis 56 Basal Cell 56 Intussusception 56 Polycystic Ovary Syndrome 56 Li Fraumeni syndrome 56 diabetic kidney 56 type2 diabetes 56 nephritis 56 breast cancer metastasis 56 multisystem disease 56 Lafora disease 56 recessive genetic 56 thrombophilia 56 Neurofibromatosis type 56 acute lymphoid leukemia 56 polycystic 56 MYH9 gene 56 type 1diabetes 56 acute lymphoblastic 56 familial hypercholesterolaemia FH 56 incurable genetic 56 paraganglioma 56 idiopathic PAH 56 hyperparathyroidism 56 enterocolitis 56 susceptibility gene 56 dominantly inherited 56 Genetic variants 56 multiple sclerosis lupus 56 Prostatitis 56 LRRK2 mutations 56 Hurthle cell 56 systemic amyloidosis 56 Vitamin B# deficiency 56 blood clotting disorder 56 myotonic dystrophy 56 NOTCH1 56 juvenile myelomonocytic leukemia 56 herpes simplex encephalitis 56 Fatty liver 56 overactive thyroid gland 56 Hypothyroidism 56 chromosomal defect 56 V Leiden 56 Brugada syndrome 56 choriocarcinoma 56 myelogenous leukemia 56 chronic autoimmune disorder 56 enterovirus infection 56 epigenetic changes 56 urethritis 56 Heavy menstrual bleeding 56 sarcoid 56 genetic abnormality 56 Autoimmune disorders 56 hyperemesis 56 renal scarring 56 spongiform encephalopathies 56 familial adenomatous polyposis FAP 56 immunodeficiency 56 nonhereditary 56 blastoma 55 endometrial hyperplasia 55 elevated CRP 55 uterine tumors 55 acute porphyria 55 bronchogenic carcinoma 55 nephrosis 55 malignant neoplasm 55 monogenic 55 Raynaud syndrome 55 abnormal pap smear 55 klotho 55 neurocysticercosis 55 mycobacterial infection 55 interstitial pneumonitis 55 Brugada Syndrome 55 overactive gland 55 Endometrial cancer 55 de ath 55 acute myeloid 55 Epstein Barr Virus 55 Pulmonary hypertension 55 TCF#L# gene 55 CMV infection 55 microscopic colitis 55 abnormal Pap test 55 apoE4 55 Hypertrophic cardiomyopathy 55 AAT deficiency 55 Aortic stenosis 55 degenerative disorder 55 hypertrophic cardiomyopathy HCM 55 undiagnosed celiac disease 55 Kufs disease 55 spinocerebellar ataxia 55 deletion 5q 55 MCAD deficiency 55 mycosis fungoides 55 Retinoblastoma 55 LRP5 55 gastro oesophageal reflux disease 55 Nephrogenic Systemic Fibrosis NSF 55 Hirschsprung disease 55 smoldering myeloma 55 Chronic fatigue 55 cirrhosis liver failure 55 septicemic 55 chorioamnionitis 55 oral thrush 55 neuro degenerative disease 55 ANCA associated 55 fatal neuromuscular disorder 55 congenital disorders 55 Acute pancreatitis 55 idiopathic pulmonary arterial hypertension 55 Genital herpes 55 inherited retinal degeneration 55 galactosemia 55 HbF 55 renovascular hypertension 55 angiosarcoma 55 sporadic Creutzfeldt Jakob 55 ARVD 55 hereditary spastic paraplegia 55 irreversible blindness 55 uncurable 55 lymphangioleiomyomatosis LAM 55 polymyalgia 55 hyperinsulinism 55 chronic obstructive airway 55 gene BRCA2 55 ectodermal dysplasia 55 autosomal dominant inheritance 55 acute rheumatic fever 55 Hurler syndrome 55 Genetic predisposition 55 lactase deficiency 55 CDH1 55 polymyalgia rheumatica 55 Vitamin D insufficiency 55 basal cell nevus syndrome 55 recurrent miscarriages 55 autistic regression 55 Reye syndrome 55 malignant hyperthermia 55 testicular cancers 55 inherited genetic mutations 55 autoimmune thyroid 55 Henoch purpura 55 susceptibility alleles 55 hepatic toxicity 55 pleural mesothelioma 55 Proteus syndrome 55 paraneoplastic 55 hypovitaminosis D 55 K ras mutations 55 Severe Combined Immunodeficiency 55 streptococcus infection 55 idiopathic epilepsy 55 pilocytic astrocytomas 55 necrotising 55 lobular breast cancer 55 Zinc deficiency 55 sporadic ALS 55 gastrointestinal stromal tumor 55 histiocytosis 55 skeletal malformations 55 interstitial nephritis 55 diease 54 elevated triglyceride levels 54 Polycystic Ovarian Syndrome PCOS 54 Acute myeloid leukemia 54 cardiac insufficiency 54 Eisenmenger syndrome 54 leptin deficiency 54 Myopathy 54 polycystic ovary syndrome 54 lactose malabsorption 54 oesophageal adenocarcinoma 54 Chronic inflammation 54 pseudotumor cerebri 54 systemic mastocytosis 54 chromosomal aberrations 54 arrhythmogenic right 54 holoprosencephaly 54 bile duct cancers 54 immunodeficiency disorder 54 hypokalemia hypomagnesemia 54 polycystic ovarian syndrome PCOS 54 Spinal muscular atrophy 54 mesotheliomas 54 dysautonomia 54 Systemic lupus erythematosus 54 enzyme deficiency 54 Intestinal parasites 54 gastrointestinal stromal tumors GISTs 54 Peanut allergy 54 multifactorial disease 54 Myalgic Encephalomyelitis 54 leiomyomas 54 Adenocarcinoma 54 XMRV infection 54 abnormal mammogram 54 EBV infection 54 bullous 54 immunodeficient 54 Toxoplasmosis 54 CMV infections 54 Recurrences 54 hereditary deafness 54 cardiac fibrosis 54 MGUS 54 spontaneous mutation 54 APOE4 54 Hutchinson Gilford progeria 54 haemochromatosis 54 ovulatory cycles 54 RPE# 54 Polycystic ovary syndrome PCOS 54 thyroid dysfunction 54 Wilms tumor 54 FTLD 54 myalgic encephalomyelitis ME 54 genetic syndromes 54 Genetic variation 54 ductal adenocarcinoma 54 Cockayne syndrome 54 BRCA2 gene mutation 54 nonalcoholic steatohepatitis NASH 54 Hemolytic Uremic Syndrome HUS 54 degenerative neurological disease 54 ovarian hyperstimulation syndrome OHSS 54 variable immunodeficiency 54 JAK mutations 54 advanced adenoma 54 Chlamydia pneumoniae 54 PTLD 54 molecular abnormalities 54 Uterine cancer 54 Cerebral malaria 54 bowel polyps 54 PTPN# 54 Mycoplasma pneumoniae 54 Leber congenital amaurosis 54 genetic alteration 54 GSTM1 gene 54 bacterium Neisseria meningitidis 54 genetic variants associated 54 ApoE gene 54 MEF2A 54 Pancreatitis 54 fat malabsorption 54 Hemochromatosis 54 Meckel Gruber 54 mtDNA mutations 54 testicular germ cell 54 SOD2 gene 54 endocrine tumors 54 Chronic lymphocytic leukemia 54 T1DM 54 Squamous 54 pernicious anemia 54 Salmonella typhi 54 abnormal proteins 54 untreated sleep apnea 54 etiologic agent 54 neovascularisation 54 Metastatic breast cancer 54 cardiac channelopathies 54 Hirschsprung Disease 54 chronic myeloid 54 GABHS 54 unprovoked seizures 54 aortic rupture 54 symptomless 54 Aplastic anemia 54 Fatty Liver Disease 54 epididymitis 54 haemolytic anemia 54 multi infarct dementia 54 Uveal melanoma 54 ApoE4 gene 54 Leber congenital amaurosis LCA 54 TGFBR1 * 6A 54 pulmonary hypertension PH 54 mutated BRCA1 54 peritoneal cancer 54 developmental abnormalities 54 chromosomal anomaly 54 Parkinson disease neurological disorder 54 hydrops 54 bowel cancers 54 #q#.# [001] 54 Li Fraumeni 54 germline mutation 54 Von Willebrand disease 54 Severe Asthma 54 autoimmune thyroiditis 54 ALI ARDS 54 underlying pathophysiology 54 prostate adenocarcinoma 54 tricuspid atresia 54 Retinitis Pigmentosa RP 54 allergic eczema 54 BRCA2 gene 54 Adjuvant chemotherapy 54 undergoing hysterectomy 54 NOD2 54 acute myocarditis 54 autoimmune hemolytic anemia 54 cholangiocarcinoma 54 Ulcerative colitis 54 airway constriction 54 ovarian malignancy 54 thiopurine 54 congenital diaphragmatic hernia 54 Sjogren Syndrome 54 obliterans 54 immunodeficiency disease 54 somatic mutations 54 Waldenstrom macroglobulinemia 54 pulmonary thromboembolism 54 cutaneous lupus 54 gonococcal infection 54 atrophic gastritis 54 moyamoya 54 cancer metastasizes 54 Porphyria 53 chronic heartburn 53 Myelodysplastic syndromes 53 Myasthenia gravis 53 monozygotic twin 53 flaccid paralysis 53 Gorlin syndrome 53 arterial calcification 53 Reye Syndrome 53 achalasia 53 Pericarditis 53 Alzheimers disease 53 unexplained mental retardation 53 pheochromocytoma 53 Fistulas 53 inherited neurological disorder 53 BARD1 53 sclerosis ALS 53 PPCM 53 tumor suppressor protein 53 oral squamous cell 53 thyroiditis 53 heartburn GERD 53 cancerdefine 53 autoimmune pancreatitis 53 spastic paraplegia 53 prosopagnosia 53 autosomal dominant disorder 53 Chlamydia trachomatis 53 hyperemesis gravidarum 53 airway hyperresponsiveness 53 thyroid tumors 53 Sjögren syndrome 53 gene mutation 53 Cellulitis 53 Folic acid deficiency 53 MSH2 53 aphthous stomatitis 53 Glioma 53 dermatologic reactions 53 calcium oxalate stones 53 chromosomal disorder 53 cerebral infarction 53 metabolic dysfunction 53 intestinal inflammation 53 neuroblastoma tumor 53 BMPR2 53 HBeAg negative 53 gynecologic malignancy 53 Malignant glioma 53 Peripheral neuropathy 53 Torsades de Pointes 53 progressive neurodegenerative disorder 53 amenorrhoea 53 Iron deficiency anemia 53 systemic scleroderma 53 Rh positive 53 Crohns disease 53 G#S mutation 53 bacteriuria 53 autoinflammatory diseases 53 gastrointestinal reflux 53 Testicular cancer 53 transfusion syndrome 53 polycystic ovaries 53 chronic hepatitis cirrhosis 53 Niemann Pick disease 53 autosomal recessive disease 53 molar pregnancy 53 virus XMRV 53 osteosarcomas 53 neurological degeneration 53 ependymoma 53 gastro esophageal reflux 53 recurrent wheezing 53 Irritable bowel syndrome 53 chromosomal mutations 53 chlamydial infection 53 ventricular dysplasia 53 Candida infection 53 Periodontal disease 53 autosomal recessive 53 pancreatitis inflammation 53 varicella infection 53 Barrett esophagus BE 53 polyp recurrence 53 human metapneumovirus 53 Oesophageal 53 BRCA carriers 53 NOMID 53 thrombotic thrombocytopenic purpura TTP 53 bacterial prostatitis 53 cholestasis 53 APOE ε4 53 progressive neurodegenerative 53 dopamine receptor gene 53 Reiter Syndrome 53 Thyroid disorders 53 antiphospholipid syndrome 53 embryonal rhabdomyosarcoma 53 Myelodysplastic Syndrome 53 hemolytic anemia 53 subfertility 53 von Hippel Lindau 53 Polycythemia vera 53 renal carcinoma 53 abnormal vaginal bleeding 53 tubercle bacillus 53 hereditary hemorrhagic telangiectasia 53 Leber Hereditary Optic Neuropathy 53 Hypoglycemia 53 Cytomegalovirus 53 LRAT 53 Wwox 53 GIST tumors 53 acetaminophen toxicity 53 germline mutations 53 brain lesions 53 degenerative neurological disorder 53 recessive trait 53 preserved ejection fraction 53 hypogonadotropic hypogonadism 53 intestinal polyps 53 erythema nodosum 53 vulvodynia 53 dermopathy 53 herpes zoster 53 nasopharyngeal carcinoma 53 serous ovarian cancer 53 Pompe Disease 53 thyrotoxicosis 53 Septicaemia 53 sCJD 53 XMRV virus 53 eosinophilic 53 gallstone formation 53 gastric adenocarcinoma 53 autosomal dominant 53 Malignant mesothelioma 53 neuropsychiatric disorder 53 BRCA1 BRCA2 53 Pemphigus 53 myelomeningocele 53 basal cell carcinoma BCC 53 Aeromonas 53 lung metastasis 53 fungus Cryptococcus neoformans 53 EoE 53 NF1 53 genetic abnormalities 53 Myocardial infarction 53 heterotaxy 53 Dilated cardiomyopathy 53 APOE e4 53 leukoencephalopathy 53 APOE e4 gene 53 BCL#A 53 persistent pulmonary hypertension 53 benign proliferative breast 53 Pleural Mesothelioma 53 RAS mutations 53 APOL1 53 recurrent infections 53 bladder cancers 53 alzheimer disease 53 Angioedema 53 Leber Congenital Amaurosis LCA 53 leukaemias 53 #q# deletion 53 fungal meningitis 53 Benign breast 53 secondary bacterial infections 53 thrombocytosis 53 T1D 53 thunderclap headache 53 malignant brain 53 Lymphocytic 52 potentially modifiable 52 Retinitis pigmentosa 52 temporal arteritis 52 retinal dysfunction 52 LKB1 52 dysgenesis 52 nerve degeneration 52 Helicobacter 52 post transplant lymphoproliferative 52 inflammatory polyarthritis 52 Chronic Fatigue Syndrome CFS 52 precancer 52 neuroblastomas 52 Motor neurone disease 52 benign polyps 52 cardiac tamponade 52 alpha thalassemia 52 Gastric cancer 52 mutated gene 52 megacolon 52 motor neuron degeneration 52 malarial infection 52 Colon polyps 52 hyperinsulinemia 52 epigenetic alterations 52 primary progressive aphasia 52 Acute Myelogenous Leukemia 52 rheumatic disease 52 Candidiasis 52 congenital anomaly 52 BRCA1 mutations 52 ApoE4 52 PAOD 52 genetic polymorphisms 52 overt hypothyroidism 52 medulloblastomas 52 Gliomas 52 LHRH receptor positive 52 autosomal dominant polycystic kidney 52 erythematosus 52 pheochromocytomas 52 motor neuron diseases 52 uremia 52 coagulation abnormalities 52 Staphylococcus aureus infections 52 Wegener granulomatosis 52 IDH mutations 52 cardiac hypertrophy 52 eosinophilic inflammation 52 myeloid leukemia 52 pituitary adenoma 52 Krabbe Disease 52 ductal breast cancer 52 pre cancerous growths 52 Shy Drager syndrome 52 premalignant lesions 52 portal vein thrombosis 52 Otitis 52 immunosuppressed 52 Aortic dissection 52 Urticaria 52 lupus scleroderma 52 idiopathic pulmonary 52 latent celiac disease 52 LRRK2 gene 52 genetically susceptible 52 debilitating neurological disorder 52 alpha1 antitrypsin deficiency 52 Excessive daytime sleepiness 52 JAK2 enzyme 52 Wiskott Aldrich syndrome 52 NKX2 52 GISTs 52 lymphoblastic lymphoma 52 metapneumovirus 52 BCR ABL protein 52 necrotizing pneumonia 52 genetic mutation 52 choroidal vasculopathy 52 Relapsing remitting MS 52 missense mutation 52 lupus erythematosus 52 lactic acidosis 52 carcinoid 52 osteosarcoma bone 52 Contraceptive pill 52 intracerebral haemorrhage 52 impair fertility 52 mutated genes 52 inflammatory bowel disease 52 vitamin B# deficiency 52 Ankylosing spondylitis 52 SSc 52 otitis 52 SIRT1 gene 52 immunocompetent 52 neural tube defect 52 kidney fibrosis 52 Campylobacter infection 52 Moraxella catarrhalis 52 Inflammatory Bowel 52 diffuse intrinsic pontine glioma 52 unexplained infertility 52 Rheumatic fever 52 lung fibrosis 52 debilitating autoimmune 52 clinically detectable 52 anovulation 52 HER2 overexpression 52 CP CPPS 52 CFTR gene 52 cancerous polyp 52 Hypophosphatasia 52 MTHFR 52 neonatal lupus 52 chromosomal alterations 52 Usher Syndrome 52 diffuse gastric 52 Atopic dermatitis 52 ischemic colitis 52 chlamydial 52 Sarcoidosis 52 apolipoprotein E gene 52 pyloric stenosis 52 Pulmonary fibrosis 52 recurrent miscarriage 52 colon polyp 52 nephrogenic fibrosing dermopathy 52 Gestational diabetes 52 pharyngeal cancer 52 torsade de pointes 52 ABCB1 52 iritis 52 bronchopulmonary dysplasia 52 Systemic lupus erythematosus SLE 52 Cirrhosis 52 decompensated cirrhosis 52 mitochondrial DNA mutations 52 induced cardiomyopathy 52 immune suppressing 52 mitochondrial myopathy 52 bile duct obstruction 52 Chlamydia psittaci 52 C EBP alpha 52 hemorrhagic cystitis 52 congenital abnormality 52 amebiasis 52 congenital deficiency 52 incurable ailment 52 glutamic acid decarboxylase 52 KCNH2 52 monoclonal gammopathy 52 chronic idiopathic 52 malignant lymphoma 52 leaky gut 52 Guillain Barré 52 Hemolytic Uremic Syndrome 52 Obstructive Sleep Apnoea 52 Great Imitator 52 proliferative diabetic retinopathy 52 primary biliary cirrhosis 52 predisposing factor 52 habitual snoring 52 Reye syndrome rare 52 Arrhythmogenic Right Ventricular Cardiomyopathy 52 Enlarged prostate 52 Oesophageal cancer 52 vWD 52 circulating EPCs 52 spontaneous regression 52 MYCN amplification 52 anatomical abnormalities 52 incurable neurological 52 thromboembolic disease 52 subclinical 52 interferon pathway 52 adrenal function 52 precocious puberty 52 aortic valve stenosis 52 IGFBP2 52 subclinical hyperthyroidism 52 primitive neuroectodermal tumors 52 myocardial fibrosis 52 SOD1 gene 52 Apert syndrome 52 BRCA mutation 52 mitochondrial disorders 52 Retinopathy 52 Nonalcoholic fatty liver 52 reactive airway 52 granulosa cell 52 Idiopathic 52 Hypotension 52 thoracic aortic disease 52 Peripheral arterial disease 52 Borrelia 52 Pneumocystis carinii 52 fructose intolerance 52 Cold sores 52 noncancerous prostate 52 QTc prolongation 52 allograft rejection 52 cardiac glycosides 52 Hormone pills 52 physiological abnormalities 52 genetic mutations 52 HGPS 52 androgen deficiency 52 mucormycosis 52 metastatic gastric 52 epigenetic modification 52 cerebral vascular disease 52 chromosomal abnormality 52 inherited neurodegenerative 52 congenital glaucoma 52 WNV encephalitis 52 Fibrosis 52 Legg Calvé Perthes disease 52 severe congenital neutropenia 52 Diabetic neuropathy 52 microvascular dysfunction 52 leptin resistance 52 Rh factor 52 COX2 52 undiagnosed sleep apnea 52 fulminant hepatic failure 52 polycystic ovary syndrome PCOS 52 Misdiagnosis 52 microvascular disease 52 herpes infection 52 Leydig cell 52 tertiary syphilis 52 Colorectal cancers 52 parasite Plasmodium falciparum 52 Pre eclampsia 52 prematurity ROP 52 Crohns Disease 52 facioscapulohumeral muscular dystrophy 52 Severe Primary IGFD 52 Esophagitis 52 obstructive pulmonary disease 51 muscle degeneration 51 elevated uric acid 51 VHL gene 51 Aviptadil 51 Appendicitis 51 cerebral atrophy 51 cranial irradiation 51 congenital deafness 51 sonographic diagnosis 51 supratentorial 51 subclinical disease 51 allelic variants 51 obstructive coronary 51 microdeletions 51 elevated cortisol 51 thoracic aortic aneurysm 51 valvular heart disease 51 Insulin resistance 51 Acid reflux 51 ovarian hormones 51 celiac patients 51 genes predisposing 51 irregular heartbeat atrial fibrillation 51 MC1R 51 Leptospira 51 mosaicism 51 GSTT1 51 ataxia telangiectasia 51 curable cancers 51 carotid stenosis 51 Hip dysplasia 51 periodontal infection 51 prostate carcinogenesis 51 ulcerative colitis Crohn disease 51 myelopathy 51 Raynaud phenomenon 51 ruptured aneurysms 51 basal cell skin 51 colorectal carcinoma 51 CMV retinitis 51 Creutzfeldt Jacob 51 MDR tuberculosis 51 Gluten intolerance 51 atopic 51 hypovolemic shock 51 Genetic variations 51 bronchoalveolar 51 uterus womb 51 alcoholic hepatitis 51 benign positional vertigo 51 thyrotropin 51 neurodegenerative disorder 51 Glioblastoma Multiforme GBM 51 Persistent Pulmonary Hypertension 51 toxoplasma 51 GATA4 51 histological subtype 51 hormonal disorder 51 Leber hereditary optic neuropathy 51 incidentalomas 51 tapeworm infection 51 atypical hemolytic uremic syndrome 51 lacunar 51 inherit predisposition 51 abnormal growths 51 pituitary tumors 51 congenital adrenal hyperplasia CAH 51 hemochromatosis 51 KIBRA 51 Chronic Pelvic Pain 51 toxocariasis 51 nonischemic 51 angiographically 51 estrogen deficiency 51 Variant Creutzfeldt Jakob Disease 51 PTEN gene 51 roseola 51 glucocorticoid therapy 51 pharmacologic intervention 51 disease vCJD 51 Diverticulosis 51 Alport syndrome 51 celiac sprue 51 infantile hemangioma 51 chronic prostatitis 51 chronic rheumatic 51 malignant pleural mesothelioma 51 cerebri 51 Acute Renal Failure 51 Polycythemia 51 ADAM# 51 endostatin 51 immunopathology 51 dermatitis herpetiformis 51 Viral infections 51 haemorrhagic 51 neurofibromas 51 aciduria 51 atypical parkinsonism 51 Valproate 51 cerebellar hypoplasia 51 subarachnoid haemorrhage 51 BRCA deficient 51 microchimerism 51 CHD7 51 choroidal melanoma 51 silent myocardial ischemia 51 Trichomonas vaginalis 51 rhinovirus infection 51 ovariectomy 51 Mucositis 51 GPC5 51 CHEK2 51 frontotemporal dementia 51 Joubert syndrome 51 mitochondrial dysfunction 51 Sanfilippo Syndrome 51 LHON 51 Vascular dementia 51 prion disease 51 B7 H3 51 Kawasaki Disease 51 Graves ophthalmopathy 51 Alzheimer Disease AD 51 Myelodysplastic syndrome 51 unstable detrusor muscle 51 celiac disease digestive 51 primary pulmonary hypertension 51 GAB2 51 MALT lymphoma 51 cardiac dysfunction 51 Autoimmune diseases 51 Primary Pulmonary Hypertension 51 hyperammonemia 51 chromosomal anomalies 51 latent TB infection 51 NF2 51 nondemented 51 Dwarfism 51 Lou Gehrigs disease 51 Cysts 51 ovarian tumors 51 Lichen planus 51 fulminant hepatitis 51 multidrug resistance 51 medulloblastoma tumors 51 Wilms tumors 51 neurological complications 51 Celiac sprue 51 pelvic irradiation 51 Excessive sweating 51 nonmelanoma skin cancer 51 meningoencephalitis 51 Pneumococcal pneumonia 51 leukemia ALL 51 juvenile idiopathic arthritis 51 IPAH 51 biochemical abnormalities 51 hematopoietic cancers 51 Opportunistic infections 51 olfactory dysfunction 51 gastroesophageal reflux GERD 51 ichthyosis vulgaris 51 intracranial haemorrhage 51 Hemophilia B 51 Ischaemic heart 51 abdominal abscesses 51 neurological abnormalities