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(Click for frequent words.) 68 congenital disorders 64 inherited retinal degeneration 63 genetic syndromes 63 chromosome abnormality 62 cardiac channelopathies 62 systemic scleroderma 62 degenerative neurological diseases 62 monogenic 62 muscular dystrophies 61 Coeliac disease 61 G6PD deficiency 61 aneuploidies 61 Spinal muscular atrophy 61 genetic defects 61 Cystic fibrosis CF 61 Vitamin B# deficiency 60 Hereditary angioedema HAE 60 lysosomal diseases 60 dominantly inherited 60 holoprosencephaly 60 DiGeorge syndrome 60 multiorgan 60 Brugada Syndrome 60 recessive genetic 60 chromosomal disorders 60 anemias 60 autoimmune hemolytic anemia 60 immunodeficiencies 60 Lafora disease 60 thyroid dysfunction 59 Hereditary angioedema 59 primary immunodeficiencies 59 chromosomal defect 59 immunodeficiency disorder 59 thyroid deficiency 59 herpesviruses 59 IgA deficiency 59 medium chain acyl 59 neuro degenerative disorders 59 dyskeratosis congenita 59 chromosomal anomalies 59 Hutchinson Gilford progeria 59 Periodontal disease 59 Von Willebrand disease 59 Polycystic kidney disease 59 congential 59 hereditary predisposition 59 Li Fraumeni syndrome 59 Malignant mesothelioma 59 Mitochondrial diseases 59 Autoimmune disorders 59 genetic disorders 59 valvular heart disease 59 hypertrophic cardiomyopathy HCM 59 transfusion syndrome 59 monogenic disorders 59 intestinal polyps 58 Bullous 58 Iron deficiency anemia 58 connective tissue disorders 58 Raynaud disease 58 Endometrial cancer 58 familial adenomatous polyposis 58 neuropsychiatric disorder 58 epigenetic changes 58 Hurler syndrome 58 immunodeficiency diseases 58 cystic kidney 58 Dwarfism 58 Alport Syndrome 58 mitochondrial mutations 58 genetic abnormalities 58 spinal muscular atrophy SMA 58 mitochondrial disorders 58 cystic fibrosis chronic pancreatitis 58 Niemann Pick disease 58 brain malformation 58 leptin deficiency 58 thrombophilia 58 diseases 58 mental retardation epilepsy 58 Tay Sachs thalassemia 58 hemochromatosis 58 diseases chronic granulomatous 58 discoid lupus 58 Leber congenital amaurosis LCA 58 necrotising 58 hemolytic disease 58 testicular tumors 58 de novo mutations 58 Genetic mutation 57 hemophagocytic lymphohistiocytosis 57 AAT deficiency 57 Hirschsprung disease 57 undiagnosed celiac disease 57 Hip dysplasia 57 Fanconi anemia 57 leukodystrophies 57 Krabbe Disease 57 thoracic aortic aneurysm 57 Acute myeloid leukemia 57 Candida infection 57 ectodermal dysplasia 57 modifier genes 57 Chronic sinusitis 57 Nephrogenic Systemic Fibrosis NSF 57 Myotonic dystrophy 57 myalgic encephalomyelitis ME 57 lysosomal storage diseases 57 Krabbe Leukodystrophy 57 Genetic predisposition 57 diffuse intrinsic pontine glioma 57 haemolytic anemia 57 lichen planus 57 metabolic abnormality 57 paraneoplastic 57 achromatopsia 57 limb deformities 57 spontaneous mutations 57 periodontal tissues 57 developmental abnormalities 57 Retinitis pigmentosa 57 fatal neuromuscular disorder 57 epigenetic markers 57 Rh incompatibility 57 haemochromatosis 57 heritable diseases 57 Severe Primary IGFD 57 sporadic Creutzfeldt Jakob 57 Leber Congenital Amaurosis LCA 57 hydatid disease 57 CHARGE syndrome 57 necrotizing pneumonia 57 dysautonomia 57 iritis 57 diease 57 Aplastic anemia 57 congenital anomaly 57 toxoplasmosis 57 hereditary deafness 57 microdeletion 57 Periodontitis 57 CMV infections 57 cutaneous lupus 57 disorder thalassemia 57 cysticercosis 57 Viral infections 57 candida infections 57 channelopathies 57 Brugada syndrome 57 Wegener granulomatosis 57 Aortic stenosis 57 alpha thalassemia 57 Chronic lymphocytic leukemia 57 Fanconi Anemia 57 Kufs disease 56 ANCA associated 56 bone deformities 56 pilocytic astrocytomas 56 Vitamin D insufficiency 56 Hemochromatosis 56 hereditary hemochromatosis 56 leukoencephalopathy 56 deafness neurological 56 Rh factor 56 genetic defect 56 pyloric stenosis 56 clefting 56 myopathies 56 urologic diseases 56 mtDNA mutations 56 NPHP 56 systemic amyloidosis 56 Beta thalassemia 56 autoinflammatory diseases 56 Tay Sachs Disease 56 Hashimoto thyroiditis 56 APOL1 56 recessively inherited 56 macular degeneration diabetic retinopathy 56 biochemical abnormalities 56 hemolytic anemia 56 recessive trait 56 Eisenmenger syndrome 56 Tay Sachs disease 56 epiglottitis 56 Zinc deficiency 56 Compulsive hoarding 56 motor neuron degeneration 56 nongenetic 56 bacterium Streptococcus pneumoniae 56 secondary bacterial infections 56 incurable neurodegenerative disease 56 bacterial endocarditis 56 Diamond Blackfan anemia 56 Intestinal parasites 56 dystrophy 56 neurodegenerative disorder 56 Genetic variants 56 thoracic aortic disease 56 chronic degenerative diseases 56 Leber congenital amaurosis 56 Neurodegenerative diseases 56 recurrent miscarriages 56 RDEB 56 urolithiasis 56 Myasthenia gravis 56 autoimmune uveitis 56 autosomal dominant disorder 56 hereditary blindness 56 arterial calcification 56 microdeletions 56 Genital herpes 56 Dental caries 56 Medulloblastoma 56 hormonal abnormalities 56 Meckel Gruber 56 ciliopathies 56 autosomal recessive 56 chronic autoimmune disorder 56 chromosomal anomaly 56 mycosis 56 mitochondrial disease 56 Joubert syndrome 56 variable immunodeficiency 56 hip dysplasia 56 aortic rupture 56 rheumatic disease 56 neuro developmental disorders 56 Fungal infections 56 CDH1 56 Rheumatic fever 55 choriocarcinoma 55 myelomeningocele 55 JAK mutations 55 Maroteaux Lamy syndrome 55 Retinoblastoma 55 Toxoplasmosis 55 Dilated cardiomyopathy 55 nonsense mutations 55 untreated celiac disease 55 spinal muscle atrophy 55 renovascular hypertension 55 MCAD deficiency 55 pneumonia septicemia 55 hereditary diseases 55 Churg Strauss syndrome 55 galactosemia 55 inherited neurological disorder 55 neurodevelopmental disorder 55 aortic dissections 55 protein misfolding diseases 55 Interstitial cystitis 55 molar pregnancy 55 aniridia 55 Lesch Nyhan syndrome 55 inherited retinal 55 periodontal gum disease 55 A. fumigatus 55 Motor neurone disease 55 craniofacial abnormalities 55 Polycystic ovary syndrome PCOS 55 congenital deafness 55 chronic granulomatous disease 55 ADAMTS# 55 Polymorphic Ventricular Tachycardia CPVT 55 genetic abnormality 55 degenerative neurological disease 55 mitochondrial diseases 55 lymphocytic choriomeningitis virus 55 mycosis fungoides 55 chromosomal alterations 55 BRAF gene 55 Heartworm disease 55 unruptured aneurysm 55 Pompe Disease 55 familial hypercholesterolaemia FH 55 muscular dystrophy cystic fibrosis 55 Von Hippel Lindau 55 Benign tumors 55 S. aureus infection 55 autosomal dominant polycystic kidney 55 chromosomal aberrations 55 incurable genetic 55 enzyme deficiency 55 facioscapulohumeral muscular dystrophy 55 Necrotizing fasciitis 55 causative genes 55 congenital adrenal hyperplasia CAH 55 Coronaviruses 55 optic atrophy 55 Lou Gehrigs disease 55 Hypertrophic 55 Mitral regurgitation 55 chronic renal disease 55 celiac sprue 55 cardiopulmonary bypass surgery 55 spastic paraplegia 55 bone deformity 55 mucormycosis 55 congenital hypothyroidism 55 Overactive bladder 55 rheumatic diseases 55 lipomas 55 Psoriatic arthritis 55 severe malignant osteopetrosis 55 connective tissue diseases 55 prenatally diagnosed 55 aortic aneurysms 55 Muscular dystrophy 55 multisystem disease 55 LQTS 55 Aortic aneurysms 55 myotonic muscular dystrophy 55 Neurofibromatosis type 55 Crohns disease 55 inherited predisposition 55 Gliomas 55 enterovirus infection 55 Chronic insomnia 55 Hurthle cell 55 polydactylism 55 recessive inheritance 55 fatal neurodegenerative 55 CHDs 55 autosomal recessive disease 55 susceptibility gene 55 Peripheral artery disease 55 JAK2 mutation 55 idiopathic pulmonary 55 acute rheumatic fever 55 Polycystic Ovarian Syndrome PCOS 55 MYH9 gene 55 paraganglioma 55 glomerulonephritis 55 VCFS 55 ataxias 55 vasa previa 55 Trichomonas 55 Chlamydia pneumoniae 55 hematologic disorders 55 atopic diseases 55 diaphragmatic hernia 55 Fragile X Syndrome 55 Hypertrophic cardiomyopathy 55 Peripheral neuropathy 55 polycystic ovarian syndrome PCOS 55 genetic lysosomal storage 55 immunodeficiency 55 CHD7 55 Malignant glioma 55 Systemic lupus erythematosus 55 molecular abnormalities 55 bacterium Neisseria meningitidis 55 Cytomegalovirus CMV 55 Infant botulism 55 allergic dermatitis 55 progressive neurodegenerative 55 Li Fraumeni 55 Cryptococcus neoformans 55 RPE# 55 polymyalgia 55 encephalitis meningitis 54 juvenile myelomonocytic leukemia 54 synovial cells 54 Androgenetic alopecia 54 LVNC 54 polyps growths 54 neuro degenerative disease 54 Alport syndrome 54 skeletal dysplasia 54 lupus multiple sclerosis 54 Hirschsprung Disease 54 Cockayne syndrome 54 chromosomal disorder 54 Pulmonary arterial hypertension 54 autoimmune thyroid 54 hemoglobinopathies 54 Heavy menstrual bleeding 54 deCODE Glaucoma TM 54 Systemic lupus erythematosus SLE 54 prematurity ROP 54 herpes infection 54 IgA nephropathy 54 anatomical abnormalities 54 ovarian hyperstimulation syndrome OHSS 54 hormonal disorder 54 embryonal rhabdomyosarcoma 54 spongiform encephalopathies 54 fibroma 54 mosaicism 54 microchimerism 54 degenerative disorder 54 Hurler Syndrome 54 PTEN mutations 54 megacolon 54 histiocytosis 54 uremia 54 hereditary spastic paraplegia 54 cortical dysplasia 54 QuantiFERON 54 neuro degenerative disorder 54 protein misfolding 54 Autoimmune diseases 54 NOMID 54 ataxia telangiectasia 54 epidermolysis bullosa EB 54 Aicardi syndrome 54 fatal neurodegenerative disorder 54 degenerative neurological disorder 54 arthropathy 54 skeletal malformations 54 staphylococcal infections 54 reproductive endocrine 54 vWD 54 spinocerebellar ataxia 54 immuno deficiency 54 Fragile X gene 54 hydrops 54 neurofibroma 54 opportunistic pathogens 54 strep bacteria 54 cerebri 54 Onychomycosis 54 herpes viruses 54 Cerebral malaria 54 long QT syndrome 54 lymphatic vasculature 54 debilitating neurodegenerative disorder 54 Leber hereditary optic neuropathy 54 rheumatic disorders 54 Retinitis Pigmentosa RP 54 Tay Sachs neurological 54 leiomyoma 54 sickle cell cystic fibrosis 54 genomic variants 54 retinal dysfunction 54 Pseudomonas aeruginosa infections 54 demyelinating disease 54 keloid scars 54 Melasma 54 streptococcus infection 54 hormonal disorders 54 myelofibrosis polycythemia vera 54 coccidia 54 genetically inherited 54 Folic acid deficiency 54 incidentalomas 54 Pericarditis 54 #q# deletion 54 Candidiasis 54 Prion diseases 54 Chronic inflammation 54 Myocarditis 54 Bacterial infections 54 Ankylosing spondylitis 54 acute myocarditis 54 meningitis encephalitis 54 filaggrin 54 feline leukemia virus 54 Equine piroplasmosis 54 Pneumococcal pneumonia 54 thiopurine 54 Male pattern baldness 54 pseudogout 54 Hyperthyroidism 54 somatic mutation 54 skeletal fluorosis 54 Apert syndrome 54 predisposing factor 54 Polycythemia vera 54 sarcoid 54 leukodystrophy 54 Fatty liver 54 chromosome rearrangements 54 hamartomas 54 Celiac sprue 54 diphtheria pertussis whooping cough 54 Langerhans cell histiocytosis 54 Krabbe leukodystrophy 54 cerebellar hypoplasia 54 neural disorders 54 bicuspid valve 54 Morbid obesity 54 Niemann Pick 54 inherited mutations 54 achalasia 54 hyperparathyroidism 54 Cancer cachexia 54 induced cardiomyopathy 54 Fanconi anemia FA 54 feline heartworm disease 54 bronchopulmonary dysplasia BPD 54 malignant lymphomas 54 Primary immunodeficiency 54 inheritable diseases 54 Magnesium deficiency 54 biphosphonates 54 suppurative 54 pituitary disorders 54 Cystic fibrosis 54 congenital birth defects 54 mycotic 54 Acromegaly 54 olfactory dysfunction 54 hereditary disorder 54 BRCA2 gene 54 Newborn screening 54 recurrent laryngeal nerve 54 Duchene muscular dystrophy 54 yeast overgrowth 54 polycystic kidneys 54 molybdenum cofactor deficiency 54 skeletal metastases 54 tick borne infections 54 DiGeorge Syndrome 54 multifactorial disease 54 cerebral vasospasm 54 progressive neurodegenerative disorders 54 Bacterial infection 54 Hemolytic Uremic Syndrome 53 epilepsies 53 ADPKD 53 Urinary tract infection 53 polyomavirus nephropathy 53 inheritable genetic 53 VHL gene 53 ADA SCID 53 uncurable 53 aspergillosis 53 dentinal hypersensitivity 53 metabolic derangement 53 respiratory syndrome virus 53 recurrent bladder 53 renal fibrosis 53 reproductive abnormalities 53 dysplastic lesions 53 chorioamnionitis 53 genetic determinants 53 ocular disorders 53 Usher Syndrome 53 diagnosed prenatally 53 fungus Cryptococcus neoformans 53 Pulmonary hypertension 53 vaginitis 53 clotting disorder 53 chronic inflammations 53 Pleural mesothelioma 53 Pseudomonas aeruginosa bacterium 53 familial ALS 53 bacterium Mycobacterium tuberculosis 53 nonmelanoma skin cancers 53 Diabetic nephropathy 53 congenital disorder 53 microbiomes 53 epididymitis 53 unknown etiology 53 spore forming bacterium 53 orchitis 53 cancerdefine 53 transmissible spongiform encephalopathies TSEs 53 neuroendocrine cancers 53 laryngeal paralysis 53 pseudotumor cerebri 53 HGPS 53 heritable genetic 53 hematological disorders 53 Valvular heart 53 cervical degenerative disc 53 Atopic dermatitis 53 dystrophies 53 idiopathic PAH 53 generalized vitiligo 53 vitamin B# deficiency 53 leukemia aplastic anemia 53 Severe Combined Immunodeficiency 53 toxocariasis 53 Anencephaly 53 Crouzon syndrome 53 hematological diseases 53 FVIII inhibitors 53 HNPCC 53 erythema nodosum 53 congenital 53 MCADD 53 Ehrlichia 53 alpha1 antitrypsin deficiency 53 retinal degenerations 53 TP# mutation 53 causative gene 53 pleural mesothelioma 53 neuro degenerative 53 benign polyps 53 congenital anomalies 53 human papillomaviruses HPV 53 degenerative disorders 53 etiologies 53 familial hypercholesterolemia 53 Bacterial vaginosis 53 epithelial tissues 53 pemphigus 53 malarial parasites 53 CMV infection 53 pelvic disorders 53 pulmonary hypertension PH 53 Candida species 53 obliterative bronchiolitis 53 germline mutations 53 Penile cancer 53 necrotizing enterocolitis NEC 53 autosomal dominant inheritance 53 Aneuploidy 53 neurological complications 53 familial polyposis 53 arrhythmogenic right 53 CFTR gene 53 genetic variants associated 53 Salmonella typhi 53 Maroteaux Lamy Syndrome 53 chlamydial 53 genes BRCA1 53 muscle dystrophies 53 histocompatibility 53 corneal dystrophy 53 diseases afflicting 53 myotonic dystrophy 53 epidermolysis bullosa 53 folic acid deficiency 53 retinal diseases 53 Crouzon Syndrome 53 oral thrush 53 otitis 53 NF1 53 Henoch purpura 53 cause cardiac channelopathies 53 Urinary incontinence 53 Alopecia areata 53 Obsessive compulsive disorder 53 ichthyosis vulgaris 53 neurologic disorders 53 Dysplasia 53 myasthenia gravis MG 53 rheumatologic 53 Thyroid nodules 53 Genetic mutations 53 atypical hemolytic uremic syndrome 53 neurofibromas 53 neurologic deficits 53 Staphylococcus aureus infections 53 Bartonella henselae 53 Male infertility 53 Crigler Najjar syndrome 53 Trichophyton rubrum 53 Neisseria meningitides 53 antifungal medications 53 transthyretin amyloidosis 53 sudden sensorineural hearing 53 Treacher Collins syndrome 53 Gluten intolerance 53 progressive neurodegenerative disorder 53 arachnoiditis 53 parasite Plasmodium falciparum 53 neurological sequelae 53 mitochondrial dysfunction 53 pharyngeal cancer 53 endocrine tumors 53 congenital diaphragmatic hernia 53 immunodeficiency disorders 53 myeloproliferative neoplasms 53 neurologic diseases 53 vascular birthmarks 53 familial pancreatic cancer 53 genetic disorder 53 LRRK2 gene 53 bacterium Borrelia burgdorferi 53 epigenetic alterations 53 Chronic fatigue 53 nerve degeneration 53 debilitating neurological disorder 53 varicella infection 53 cytomegalovirus infection 53 lysosomal storage disease 53 physiologic mechanisms 53 Pre eclampsia 53 Nasal allergies 53 idiopathic epilepsy 53 gastrointestinal dysfunction 53 chromosomal abnormalities 53 Sporadic CJD 53 Barrett esophagus precancerous 53 nonalcoholic cirrhosis 53 fungal organisms 53 paroxysmal nocturnal hemoglobinuria 53 aneuploid cells 53 congenital abnormality 53 Lactose intolerance 53 Neurological disorders 53 Lupus nephritis 53 immunosuppressed patients 53 Prostatitis 53 congenital scoliosis 53 osteogenesis imperfecta OI 53 Nail fungus 53 parasitic worm infections 53 congenital blindness 53 muscular degeneration 53 C. neoformans 53 respiratory viral infections 53 leiomyomas 53 polymorphic ventricular tachycardia 53 blood clotting disorder 53 Legg Calvé Perthes disease 53 interstitial pneumonitis 53 Dental fluorosis 53 congenital CMV 53 inherited genetic mutations 53 intestinal disorders 53 nodular lesions 53 Canavan Disease 53 Osteosarcoma 53 ischemic bowel 53 nonhereditary 53 BRCA gene 53 Folate deficiency 53 progressive neuromuscular 53 Premature Ovarian Failure 53 malarial infection 53 clinically heterogeneous 53 Gynecomastia 53 Meningiomas 53 carcinoid tumor 53 WAGR syndrome 53 cardiomyopathies 53 Peritoneal mesothelioma 53 renal carcinoma 53 blood clotting disorders 53 parainfluenza virus 53 leaky gut 53 neovascularisation 53 Mendelian diseases 53 respiratory gastrointestinal 53 hamartoma 53 chromosome #q#.# [001] 53 periodontal infection 53 neoplastic 53 Inflammatory bowel diseases 53 chromosomal translocations 53 congenital malformations 53 lymphocytic 53 testicular dysgenesis syndrome 53 Stargardt Macular Dystrophy SMD 53 urogenital infections 52 Human papillomavirus HPV 52 Menkes disease 52 neurovascular diseases 52 TTR amyloidosis 52 adenovirus infections 52 debilitating complication 52 variant Creutzfeld Jakob 52 primary ciliary dyskinesia 52 parasitic infections 52 Loeys Dietz syndrome 52 immunocompetent 52 Meckel Gruber syndrome 52 Cockayne Syndrome 52 sCJD 52 Hemolytic Uremic Syndrome HUS 52 collagen vascular 52 rheumatoid arthritis lupus 52 post surgical adhesions 52 ARVD 52 blastoma 52 teratoma 52 somatic mutations 52 mastocytosis 52 pathologies 52 abnormal angiogenesis 52 Dravet syndrome 52 gene rearrangements 52 NF2 52 Human Papillomavirus 52 Variant Creutzfeldt Jakob Disease 52 achondroplasia 52 Chronic Prostatitis 52 Haptoglobin 52 multidrug resistance 52 brain lesions 52 inflammatory demyelinating 52 Proteus syndrome 52 etiologic factors 52 Cholangiocarcinoma 52 bronchogenic carcinoma 52 thyroiditis 52 TACI mutations 52 Muscular dystrophies 52 chromosomal defects 52 Pulmonary fibrosis 52 facial clefts 52 congenital defects 52 amyloid protein plaques 52 Congenital Adrenal Hyperplasia 52 NAGS deficiency 52 chronic sinus infections 52 beta thalassemia 52 Glioblastoma multiforme GBM 52 scleroderma chronic 52 blood coagulation disorders 52 monozygotic twin 52 Human Papilloma Virus HPV 52 histologic subtype 52 AAT Deficiency 52 enteric pathogens 52 hyperinsulinism 52 Sezary syndrome 52 CMV retinitis 52 GPC5 52 Epstein Barr virus EBV 52 von Hippel Lindau 52 neuropsychiatric diseases 52 motor neuron diseases 52 Morquio syndrome 52 arthritis lupus 52 type 1diabetes 52 Reye syndrome rare 52 Osteoarthritis OA 52 Pressure ulcers 52 unexplained mental retardation 52 ischemic mitral regurgitation 52 systemic autoimmune 52 endocrine disorder 52 Candida overgrowth 52 Wernicke Korsakoff syndrome 52 MYH9 52 craniofacial deformities 52 chronic obstructive airway 52 nonvascular 52 Sjögren syndrome 52 zoonotic pathogens 52 Latent TB 52 viral bacterial 52 neuro degenerative diseases 52 choroidal melanoma 52 syringomyelia 52 Congenital Muscular Dystrophy 52 disease CJD 52 malformation 52 genetic mutations 52 Ribavirin causes 52 varicocele 52 twin transfusion 52 transmissible spongiform encephalopathies 52 bone marrow mesenchymal stem 52 telogen effluvium 52 Pelvic inflammatory 52 eosinophilic 52 Canine influenza 52 Sanfilippo Syndrome 52 neurological degeneration 52 fetal anomalies 52 Genital warts 52 hypercoagulability 52 fronto temporal dementia 52 genetic polymorphisms 52 intravascular coagulation 52 retinal vascular 52 ependymoma 52 calf scours 52 heartworm infection 52 causative agents 52 Duchenne muscular dystrophy DMD 52 neuroendocrine cells 52 supratentorial 52 tricuspid atresia 52 multisystem disorder 52 Chiari malformation 52 allogeneic HSCT 52 Noonan Syndrome 52 Postherpetic neuralgia 52 organophosphate exposure 52 candida overgrowth 52 gene MECP2 52 disease 52 noncontagious disease 52 heritable disorders 52 Sandhoff disease 52 Degenerative diseases 52 pre cancerous lesion 52 Aortic valve 52 Sjogren Syndrome 52 swallowing disorders 52 nephrogenic 52 Plasmodium parasites 52 renal diseases 52 neuropsychiatric disorders 52 MEF2A 52 invasive fungal infection 52 post transplant lymphoproliferative 52 Bardet Biedl syndrome 52 gene BRCA2 52 swine dysentery 52 Multiple sclerosis MS 52 alveolar rhabdomyosarcoma 52 cystic fibrosis hereditary 52 glial tumors 52 neuropathies 52 nonmelanoma skin cancer 52 necrotizing 52 Friedreich 52 Irritable bowel syndrome 52 Spina bifida 52 Epileptic seizures 52 familial dysautonomia 52 chronic otitis media 52 Strep infections 52 renal scarring 52 osteopetrosis 52 phenotypic variability 52 adenomatous polyps 52 Irritable bowel syndrome IBS 52 parasitic infestation 52 Smith Lemli Opitz syndrome 52 retinal degenerative disease 52 pathogenic mutations 52 precocious puberty 52 sporadic ALS 52 Acute lymphoblastic leukemia 52 hyperemesis 52 pediatric cataract 52 autoimmune thyroiditis 52 Degenerative disc disease 52 neuro developmental 52 molecular etiology 52 myiasis 52 irregular heartbeat atrial fibrillation 52 pathological hallmarks 52 hemorrhagic cystitis 52 Usher syndrome 52 neuropsychological impairments 52 enterovirus infections 52 abnormal hemoglobin 52 Takayasu arteritis 52 Osteogenesis imperfecta 52 subclinical infection 52 meningoencephalitis 52 Malignant tumors 52 malayi 52 diabetic retinopathy DR 52 Creutzfeld Jakob disease 52 rhinovirus infection 52 recurrent infections 52 ambiguous genitalia 52 bacteria Helicobacter pylori 52 myeloproliferative 52 autosomal recessive genetic 52 subfertility 52 dissociative disorders 52 CA MRSA infections 52 craniofacial defects 52 neurogenerative diseases 52 Alzhemier 52 Chronic pancreatitis 52 underactive thyroid gland 52 corneal blindness 52 genetic neuromuscular disorder 52 Huntingtons disease 52 chlamydiosis 52 gastrointestinal stromal tumor 52 venous blood clots 52 limb malformations 52 Peanut allergy 52 Fungal infection 52 Tourette Syndrome TS 52 exocrine glands 52 Wilm tumor 52 paralytic illness 52 cystic lesions 52 invasive secretory carcinoma 52 prenatal exposures 52 unprovoked seizures 52 congenital muscular dystrophy 52 ovarian malignancy 52 nephronophthisis 52 Keratitis 52 autosomal recessive disorder 52 abnormal vaginal bleeding 52 aortic valve stenosis 52 Polycystic ovary syndrome 52 thoracic aortic aneurysms 52 mycobacterial infection 52 acute lymphoid leukemia 52 placenta accreta 52 asthmas 52 Wiskott Aldrich syndrome 52 cystic fibrosis Duchenne muscular 52 osteoporotic vertebral fractures 52 microscopic colitis 52 feline distemper 52 osteochondritis dissecans 52 tonsil stones