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(Click for frequent words.) 66 Hereditary 61 heredity 54 nonhereditary 52 Von Hippel Lindau 52 heritable 51 autosomal dominant 51 genetic predisposition 51 autosomal recessive 51 familial polyposis 51 spastic paraplegia 50 multisystem disease 50 recessive genetic 50 congenital 50 galactose intolerance severe 50 hereditary predisposition 49 patrilineal 49 defective gene 49 genetically inherited 49 inheritable 49 recessive trait 49 el Kurdi 49 ataxias 49 genetic mutation 49 Li Fraumeni syndrome 49 genetic defect 49 genetic 49 mutation 48 osteodystrophy 48 TP# mutation 48 matrilineal 48 inherited genetic mutations 48 primogeniture 48 mutated gene 48 familial adenomatous polyposis FAP 48 autosomal dominant disorder 47 genes predisposing 47 dominantly inherited 47 autosomal dominant inheritance 47 Von Willebrand disease 47 paternal lineage 47 inherited 47 HNPCC 47 hereditary succession 47 achondroplasia 47 genetic susceptibility 47 chromosome deletion 47 hereditary ruler 47 familial adenomatous polyposis 47 diffuse gastric 46 genetic mutations 46 Genetic predisposition 46 male primogeniture 46 monogenic 46 Chronic pancreatitis 46 Male pattern baldness 46 retinal dysfunction 46 AAT deficiency 46 hereditary hemochromatosis 46 LRRK2 mutations 46 susceptibility gene 46 hemochromatosis 46 kingship 45 Heredity 45 inherited mutations 45 genetic syndromes 45 haemochromatosis 45 degenerative disorder 45 Retinitis Pigmentosa RP 45 chromosome abnormality 45 progressive degeneration 45 neurodegenerative disorder 45 genetic abnormality 45 congenital disorders 45 polydactylism 45 hereditary disorders 45 inherited neurological disorder 45 proband 45 incurable neurodegenerative disease 45 congential 45 blood clotting disorder 45 familial pancreatic cancer 45 gene mutation 45 Mendelian 44 Brugada syndrome 44 PTEN mutations 44 APOE ε4 44 clan chieftain 44 paraneoplastic 44 monarchical 44 myotonic dystrophy 44 lactase deficiency 44 inherited predisposition 44 Proteus syndrome 44 Vascular dementia 44 alexia 44 Fanconi anemia 44 TACI mutations 44 Shia Imami Ismaili Muslims 44 spinal muscle atrophy 44 spontaneous mutation 44 inherited retinal degeneration 44 autosomal dominant polycystic kidney 44 incurable genetic 44 Polymorphic Ventricular Tachycardia CPVT 44 osteogenesis imperfecta OI 44 progressive neurodegenerative disorders 44 apolipoprotein E gene 44 CDH1 44 consanguineous 44 Ashkenazi Jews 44 familial ALS 44 monarchic 44 Myotonic dystrophy 44 Wolf Hirschhorn 44 germline mutations 44 sporadic Creutzfeldt Jakob 44 non polyposis colorectal 44 hypertrophic cardiomyopathy HCM 44 Hashimoto thyroiditis 44 disorder thalassemia 44 Ehlers Danlos syndrome 44 Wiskott Aldrich Syndrome 44 Mendelian disorders 44 autosomal recessive disorder 44 Meckel Gruber 44 neurasthenia 43 Mendelian diseases 43 Motor neurone disease 43 JAK2 mutation 43 hereditary blindness 43 vascular Ehlers Danlos 43 chieftainship 43 Leber congenital amaurosis LCA 43 ectodermal dysplasia 43 Shy Drager syndrome 43 progressive neurodegenerative disorder 43 polydactyly 43 intestinal polyps 43 Zinc deficiency 43 Lafora disease 43 long QT syndrome 43 peptic ulcer disease 43 paraganglioma 43 subclinical hyperthyroidism 43 neural crest 43 consanguineous marriages 43 hereditary nonpolyposis colorectal cancer 43 inherited genetic mutation 43 5q 43 Saxe Coburg Gotha 43 cystic fibrosis sickle cell 43 Brugada Syndrome 43 aniridia 43 Perthes disease 43 Churg Strauss syndrome 43 AAT Deficiency 43 progressive retinal degenerative 43 feudal 43 Apert syndrome 43 recessive genes 43 hyperinsulinism 43 Neurofibromatosis type 43 de novo mutations 43 NF1 gene 43 pyloric stenosis 43 androgenetic alopecia 43 Hip dysplasia 43 Usher Syndrome 43 porphyria 43 aristocracies 43 cryptorchidism 43 hormonal disorder 43 Tay Sachs thalassemia 43 immuno deficiency 43 hypertrichosis 43 ceremonial figurehead 43 Hutchinson Gilford progeria 43 variable immunodeficiency 43 spongiform encephalopathies 43 shaking palsy 43 Maroteaux Lamy Syndrome 43 brain malformation 43 Oxidative stress 43 hereditary hemorrhagic telangiectasia 43 Aicardi syndrome 43 Angelman syndrome 43 hereditarily 43 skeletal dysplasia 43 dyskeratosis congenita 43 Hirschsprung Disease 43 ventricular cardiomyopathy 43 TCF#L# gene 43 Epileptic seizures 43 fatal neurodegenerative 43 inheritable genetic 42 hereditary spastic paraplegia 42 holoprosencephaly 42 Spinal muscular atrophy 42 immunodeficiency diseases 42 incurable neurological disorder 42 cardiac insufficiency 42 polyps growths 42 genetic disorder 42 atypical parkinsonism 42 chromosomal alterations 42 congenital abnormality 42 autosomal recessive genetic 42 erythema nodosum 42 congenital muscular dystrophies 42 Marfan syndrome 42 nongenetic 42 DiGeorge syndrome 42 Ananangya 42 Raynaud disease 42 imperfecta 42 degenerative neurological disease 42 fatal neurodegenerative disorder 42 epigenetic changes 42 recessive gene 42 idiopathic epilepsy 42 degenerative neurological disorder 42 maternally inherited 42 Hurler syndrome 42 Muscular dystrophy 42 rare chromosomal disorder 42 septo optic dysplasia 42 neurological disorder affecting 42 autosomal recessive disease 42 polygenic 42 gene 42 mutant gene 42 diabetes insipidus 42 ataxia 42 generalized epilepsy 42 atopic 42 progressive neurodegenerative disease 42 progressive neurodegenerative 42 cardiac arrythmia 42 syringomyelia 42 hereditary deafness 42 Dwarfism 42 BRCA2 gene mutations 42 cystic fibrosis Duchenne muscular 42 FTLD 42 susceptibility alleles 42 osteopetrosis 42 genetic trait 42 DICER1 42 chromosomal 42 benign proliferative breast 42 monozygotic twins 42 neuropsychiatric disorder 42 recurrent miscarriages 42 underactive thyroid gland 42 fatal neuromuscular disorder 42 congenital disorder 42 pseudotumor cerebri 42 SRY gene 42 Fatty liver 42 epidermolysis bullosa EB 42 situs inversus 42 genetic defects 42 monarchial 42 hereditary monarchy 42 lissencephaly 42 bicuspid valve 42 Hypertrophic cardiomyopathy 42 IKZF1 42 dynastic 42 consanguineous marriage 42 profound deafness 42 benign positional vertigo 42 Familial 42 hereditary diseases 42 G#S mutation 42 hepatitis B infection 42 cardiac channelopathies 42 motor neuron diseases 42 degenerative neurological 42 Lady Rai nursemaid 42 APOE gene 42 pilocytic astrocytomas 41 lateral sclerosis ALS 41 SCA5 41 predisposes 41 sCJD 41 Tay Sachs disease 41 monogenic disorders 41 missense mutations 41 neoplasias 41 GBA mutations 41 mitochondrial mutations 41 Aortic stenosis 41 paternal 41 arteriosclerosis 41 chromosomal anomaly 41 genetic disorders 41 chronicity 41 Coeliac disease 41 pattern baldness 41 Y chromosome 41 congenital cataract 41 Mental retardation 41 atopy 41 sporadic ALS 41 monarchism 41 lineage 41 gene APOE4 41 Diverticulosis 41 congenital deficiency 41 recessive inheritance 41 Pulmonary hypertension 41 genes 41 untreated celiac disease 41 Inherited 41 Retinitis pigmentosa 41 Joubert syndrome 41 premalignant 41 cryptogenic 41 Dental caries 41 GSTM1 gene 41 NF1 41 parkinsonism 41 penetrance 41 chromosomal disorder 41 incurable degenerative 41 BRCA2 gene 41 chronic obstructive airway 41 Fragile X gene 41 LRRK2 gene 41 Long QT syndrome 41 optic nerve hypoplasia 41 baronetcy 41 VCFS 41 spastic diplegia 41 fronto temporal dementia 41 hydrops 41 undescended testicle 41 autosomal 41 CCR5 delta# 41 Arthrogryposis Multiplex 41 Raynaud syndrome 41 Crouzon syndrome 41 induced cardiomyopathy 41 genetic abnormalities 41 exfoliation glaucoma 41 #p#.# [001] 41 ali'i 41 shorter telomeres 41 hereditary degenerative 41 minority Alawite 41 mutations 41 benign breast 41 non syndromic 41 Androgenetic alopecia 41 autoinflammatory diseases 41 Wet'suwet'en First 41 progressive degenerative neurological 41 amenorrhoea 41 ancestry 41 ventricular dysplasia 41 neoplastic 41 Kufs disease 41 ocular albinism 41 Dilated cardiomyopathy 41 hyperparathyroidism 41 Cowden syndrome 41 MYH9 gene 41 Usher syndrome 41 neonatal lupus 41 spinocerebellar ataxia 41 lineal descendant 41 primary progressive aphasia 41 chromosomal disorders 41 retinitis pigmentosa degenerative 41 Loeys Dietz syndrome 41 Diamond Blackfan anemia 41 Alport syndrome 41 rheumatic disease 41 gastric atrophy 41 corneal dystrophy 41 congenital scoliosis 41 congenital muscular dystrophy 41 autoimmune thyroid 41 traumatic disabling neurological 41 #q#.# [001] 41 sickle cell cystic fibrosis 41 ORMDL3 41 Cockayne syndrome 41 nerve degeneration 41 Spina bifida 41 Malignant mesothelioma 41 cervical spondylosis 41 gene variant 41 metabolic disturbances 41 gallstone disease 41 Cystic fibrosis CF 41 disease 41 rheumatic heart 41 underlying pathophysiology 41 progressive neurological disorder 41 pheochromocytomas 41 chromosomal deletions 41 cardiomyopathies 41 Krabbe Leukodystrophy 41 genetically predisposed 41 facioscapulohumeral muscular dystrophy 41 neuro degenerative 41 phenotypic expression 41 genetics 41 hereditary pancreatitis 41 maternal grandfathers 41 Sjögren syndrome 41 autoimmune thyroiditis 41 Rwenzururu kingdom 41 mutated genes 41 Pernicious anemia 41 primary biliary cirrhosis 41 earldom 41 dysgenesis 40 UGT#B# 40 Polycystic kidney disease 40 aciduria 40 #p# [001] 40 Abdul Aziz Ibn Saud 40 uro genital 40 haplotype 40 leptin deficiency 40 MECP2 gene 40 aY chromosome 40 Hyperthyroidism 40 intestinal ulcers 40 primary ciliary dyskinesia 40 nephron 40 Congenital Adrenal Hyperplasia 40 Hypertrophic 40 Klinefelter syndrome 40 familial aggregation 40 cerebellar ataxia 40 spontaneous mutations 40 adenomatous polyps 40 renal carcinoma 40 premature ovarian 40 Henoch purpura 40 muscular dystrophy cystic fibrosis 40 arteriosclerotic 40 IgA deficiency 40 Genetic susceptibility 40 breast cancer genes BRCA1 40 agenesis 40 descendant 40 colorectal polyps 40 Hutchinson Gilford Progeria 40 filaggrin 40 allelic variants 40 gall stones 40 neurodegenerative disorder characterized 40 premorbid 40 Shilubana 40 mitochondrial disorders 40 congenital abnormalities 40 Leber congenital amaurosis 40 autoinflammatory 40 aneuploidies 40 thyroid dysfunction 40 testicular germ cell 40 predisposing factor 40 SLC#A# gene [001] 40 congenital anomaly 40 Periodontal disease 40 Kingitanga movement 40 antithrombin deficiency 40 nondemented 40 alpha thalassemia 40 periodontal infection 40 gene BRCA 40 arthrogryposis 40 multigenic 40 Radiographic findings 40 hippocampal function 40 maternally transmitted 40 Leber Congenital Amaurosis LCA 40 polycystic kidneys 40 myelodysplasia 40 cardiac fibrosis 40 incomplete penetrance 40 Essential tremor 40 Hutchinson Gilford Progeria Syndrome 40 Schizoaffective disorder 40 clotting disorder 40 fibrodysplasia ossificans progressiva 40 channelopathies 40 essential thrombocythemia 40 NPM1 gene 40 subfertility 40 thalassemia sickle cell 40 obstructive coronary 40 Negroid 40 #q# [001] 40 microcephaly 40 malformations 40 FXTAS 40 aphthous stomatitis 40 cystic fibrosis chronic pancreatitis 40 neuro degenerative disorder 40 nephrosis 40 chromosomal instability 40 mosaicism 40 Moebius syndrome 40 auditory neuropathy 40 Endometrial cancer 40 ichthyosis 40 myeloproliferative 40 von Hippel Lindau 40 exfoliative glaucoma 40 eosinophilic 40 marrying Roman Catholics 40 recessive mutations 40 fatty liver disease 40 macular disease 40 Ovary removal 40 Osteogenesis Imperfecta 40 progressive degenerative 40 exotropia 40 monarchies 40 recessively inherited 40 myalgic encephalomyelitis ME 40 CYP#A# gene 40 testicular tumors 40 ADPKD 40 Hashemite dynasty 40 Arrhythmogenic Right Ventricular Cardiomyopathy 40 genes predispose 40 genomic variants 40 uncurable 40 CHARGE syndrome 40 Tourette Syndrome TS 40 predisposing factors 40 dysplasia 40 tricuspid atresia 40 Telomere length 40 Alawi sect 40 Severe Combined Immunodeficiency 40 motor neuron disease 40 velo cardio facial 40 somatic mutation 40 unexplained infertility 40 Vitamin B# deficiency 40 biological predisposition 40 Palauan passports 40 Barrett esophagus 40 genes BRCA1 40 APOE4 40 Genetic mutation 40 malignant hyperthermia 40 chromosomal imbalance 40 Epidermolysis bullosa 40 aetiological 40 systemic amyloidosis 40 genetic lysosomal storage 40 predisposition 40 Ischaemic heart 40 XMRV infection 40 thrombophilia 40 gene p# 40 liver disease 40 gene mutations 40 Hirschsprung disease 40 viral etiology 40 predispose 40 Sickle cell 40 G#S [002] 40 Chiari malformation 40 nephritis 40 PNET 40 cerebri 40 Obusinga bwa Rwenzururu 40 enterocolitis 40 priestly caste 40 microscopic colitis 40 temporal arteritis 40 highly heritable 40 spontaneous remission 40 motor neurone 40 familial 40 subclinical 40 gallstones 40 skeletal malformations 40 Hapsburg dynasty 40 monoclonal gammopathy 40 susceptibility genes 40 Vitamin D insufficiency 40 crown prince Sheik Saad 40 CHD7 40 Bovine spongiform encephalopathy BSE 40 causative genes 40 extra centrosomes 40 acute rheumatic fever 40 vitamin deficiency 40 germline 40 epididymitis 40 Beta thalassemia 40 Nwamitwa 40 basal cell nevus syndrome 40 optic atrophy 39 fibrosing cardiomyopathy 39 hypokalemia hypomagnesemia 39 Li Fraumeni 39 coexistent 39 diaphragmatic hernia 39 chromosome #q# [002] 39 FASPS 39 undergoing hormonal therapy 39 Chronic fatigue 39 hypercoagulability 39 lysosomal storage disease 39 premalignant lesions 39 dissociative amnesia 39 valvular heart disease 39 STK# gene 39 COMT gene 39 chromosomal anomalies 39 pernicious anemia 39 microdeletion 39 multifactorial 39 Chrysanthemum throne 39 Ottoman dynasty 39 fat malabsorption 39 cirrhotic liver 39 velayat e faqih 39 Hypophosphatasia 39 X chromosome 39 Anencephaly 39 Hereditary angioedema 39 VHL gene 39 neurological abnormalities 39 fructose intolerance 39 familial hypercholesterolemia FH 39 heterotaxy 39 Familial Adenomatous Polyposis FAP 39 MSH2 39 polymyositis 39 chromosomal rearrangement 39 renal fibrosis 39 polycystic ovary 39 pigmentosa 39 genetically homogeneous 39 TCF#L# 39 Shaikh Saad 39 Sudairi 39 vascular cognitive impairment 39 neurodevelopmental disorder 39 sacral agenesis 39 Rh factor 39 Nicotine dependence 39 malignant 39 absolute monarchs 39 phenotypic variation 39 Fragile X Syndrome 39 Sarcopenia 39 Lewy body 39 achromatopsia 39 nonprogressive 39 dementia praecox 39 polycystic ovary syndrome 39 klotho 39 skeletal fluorosis 39 DiGeorge Syndrome 39 pathophysiologic 39 neurological manifestations 39 familial hypercholesterolemia 39 Joubert Syndrome 39 Peripheral neuropathy 39 autonomic dysfunction 39 congenital glaucoma 39 Sjogren Syndrome 39 ARVC 39 TTR amyloidosis 39 mtDNA mutations 39 Chrysanthemum Throne 39 TMJ temporomandibular joint 39 inbreeding 39 Insulin resistance 39 V Leiden 39 nonsense mutations 39 pathognomonic 39 onset Alzheimer 39 BRCA mutation 39 Jung Bahadur Rana 39 Stargardt Macular Dystrophy 39 Syndrome SADS 39 leukodystrophies 39 hypogonadotropic hypogonadism 39 chronic autoimmune disorder 39 Colorectal cancers 39 genomic imprinting 39 hay fever allergic rhinitis 39 dynastic rule 39 immunodeficiencies 39 mitochondrial respiratory 39 pheochromocytoma 39 Hurthle cell 39 Mitochondrial DNA 39 alopecia 39 savant syndrome 39 genetic variant 39 Myocarditis 39 spondylolysis 39 #q#.# deletion syndrome 39 Myasthenia gravis 39 Chief Pleas 39 ABO blood 39 cause cardiac channelopathies 39 obstructive coronary artery 39 paragangliomas 39 MGUS 39 PALB2 39 systemic scleroderma 39 BRCA2 mutation 39 discoid lupus 39 RDEB 39 proliferative diabetic retinopathy 39 benign polyps 39 promyelocytic leukemia 39 familial clustering 39 Adiabene 39 Retinoblastoma 39 Krabbe leukodystrophy 39 chromosome 39 Tuthmosis 39 juvenile myelomonocytic leukemia 39 Hemochromatosis 39 Crouzon Syndrome 39 TP# mutations 39 inheritance 39 ancestral 39 heritable genetic 39 Systemic lupus erythematosus 39 asperger syndrome 39 Osteogenesis imperfecta 39 Bangwato 39 inherited neurodegenerative 39 cancerous polyps 39 chromosomal rearrangements 39 Lennox Gastaut syndrome 39 genetic neuromuscular disorder 39 senility 39 Y chromosomal 39 neurologic deficits 39 HFE gene 39 genomic instability 39 Telomere shortening 39 Dravet syndrome 39 clinically heterogeneous 39 neoplasm 39 renal scarring 39 germline mutation 39 GSTT1 39 childhood leukaemias 39 Parkinson disease degenerative neurological 39 eight reigning empresses 39 chromosome #q# [001] 39 VUR 39 progranulin gene 39 beta thalassemia 39 chromosomal defects 39 dopamine transporter gene 39 obesity sedentary lifestyle 39 Tibeto Burman language 39 structural abnormalities 39 peptic ulcer 39 ApoE gene 39 inheritable diseases 39 glandular 39 opsoclonus myoclonus syndrome 39 Parkinson disease degenerative 39 mental retardation epilepsy 39 Pdx1 39 monogenic diabetes 39 mitochondrial DNA 39 Ectopia Cordis 39 Prenatal diagnosis 39 Pulmonary arterial hypertension 39 pulmonary hypertension PH 39 royal bloodline 39 muscle degeneration 39 disabling neurological 39 hyperinsulinemia 39 cortical cataract 39 Inflammatory bowel disease 39 brother Belhassen 39 Peutz Jeghers syndrome 39 metachromatic leukodystrophy 39 bacteria Helicobacter pylori 39 debilitating neurodegenerative 39 roseola 39 Benign breast 39 primary sclerosing cholangitis 39 CFTR gene 39 microdeletions 39 Irritable bowel syndrome 39 ADA SCID 39 metaplasia 39 chromosomal abnormalities 39 Mitral regurgitation 39 Moebius Syndrome 39 Sturge Weber 39 neurofibroma 39 idiopathic myelofibrosis 39 gene locus 39 filaggrin gene 39 lymphatic vasculature 39 Genetic variants 39 abnormal glucose metabolism 39 paroxysmal nocturnal hemoglobinuria 39 axonal damage 39 autoimmune pancreatitis 39 Parkinson degenerative 39 Autosomal dominant 39 embryonal 39 Sheikh Saad 39 C#Y mutation 39 blindness paralysis 39 Wilms Tumor 39 FSGS 39 Tourette syndrome neurological disorder 39 periodontal disease 39 G6PD deficiency 39 Krabbe Disease 39 Shwachman Diamond Syndrome 39 Six3 39 premature senility 39 advanced glycation endproducts 39 causally linked 39 Frontal lobe 39 pyelonephritis 39 blindness deafness 39 prosopagnosia 39 phenotype 39 Zezuru 39 multisystem disorder 39 Canavan Disease 38 neurobiological disorder 38 cervical uterine 38 MEN 2B 38 OCA2 38 degenerative nerve disorder 38 LHON 38 Treacher Collins 38 polyploidy 38 Lou Gherig Disease 38 Great Imitator 38 haemorrhagic 38 Goldenhar syndrome 38 systemic mastocytosis 38 hypoplasia 38 congenital cataracts 38 huntingtin gene 38 congenital deformity 38 APOE e4 38 noncancerous 38 eosinophilic inflammation 38 liver cirrhosis 38 multi infarct dementia 38 Hypertrophic Cardiomyopathy HCM 38 Pelizaeus Merzbacher disease 38 primitive neuroectodermal tumor 38 malignancy 38 Leber hereditary optic neuropathy 38 disease NAFLD 38 Mitochondrial dysfunction 38 seigneur 38 Reflex sympathetic dystrophy 38 presumed heir 38 idiopathic 38 myeloproliferative neoplasms MPNs 38 malignant transformation 38 son Jong Un 38 Worthingtons testified 38 PTEN gene 38 ApoE4 gene 38 Ashkenazi Jewish 38 Atopic dermatitis 38 neurologic disorder 38 chromosomal aberration 38 Myelodysplastic syndrome 38 degenerative neurological condition 38 Marfan syndrome genetic 38 celiac sprue 38 BRCA1 gene 38 WAGR syndrome 38 descendants 38 urolithiasis 38 hereditary disorder 38 hypoplastic 38 mitochondrial disease 38 genetic alterations 38 bicuspid aortic valve 38 Sudden Arrhythmic Death 38 SCN9A gene 38 alveolar rhabdomyosarcoma 38 Neurofibromatosis Type 38 periodontal infections 38 fibrodysplasia ossificans progressiva FOP 38 descendents 38 Autoimmune diseases 38 ApoE4 38 cardiovascular cerebrovascular 38 neurogenic 38 diverticular disease 38 atherosclerotic cardiovascular disease 38 HLA DRB1 38 Crigler Najjar syndrome 38 potentially modifiable 38 amyloidosis 38 throne 38 imamate 38 dizygotic twins 38 hereditary nonpolyposis colon cancer 38 onset Alzheimer disease 38 bronchogenic carcinoma 38 lichen planus 38 Habsburg dynasty 38 p# mutations 38 interstitial nephritis 38 MYH9 38 Oppositional Defiant Disorder 38 deafness 38 feudal oligarchic 38 childhood leukemia 38 bowel polyps 38 Parkinsons disease 38 multiple sclerosis lupus 38 sister stepbrother stepsister 38 Foroud 38 Excessive sweating 38 Alopecia areata 38 undescended testes 38 endocrine disorder 38 husband Prince Akishino 38 neurodevelopment disorder 38 cortical dysplasia 38 H pylori 38 incurable degenerative brain 38 myocarditis inflammation 38 chronic rheumatic 38 hypotonia 38 systemic autoimmune 38 myoclonic epilepsy 38 sui juris 38 SHANK3 gene 38 de ath 38 Queen Mata'aho 38 inherited retinal 38 aldehyde dehydrogenase 38 leaky gut 38 ardent royalist 38 frontotemporal dementia 38 coronary microvascular 38 Dental fluorosis 38 McCune Albright 38 neurofibromas 38 meningitis encephalitis 38 cataracts clouding 38 degenerative 38 degenerative neuromuscular disease 38 cancerous enlargement 38 embryonal rhabdomyosarcoma 38 Rubinstein Taybi syndrome 38 APOE genotype 38 granulosa cell 38 Chronic inflammation 38 neonatal respiratory distress 38 Arnold Chiari Malformation 38 Muscular dystrophies 38 cirrhosis 38 Henry Wako Muloki 38 Urinary tract infection 38 polymyalgia 38 retinitis pigmentosa RP 38 unprovoked seizures 38 inherit predisposition 38 alleles 38 mtDNA 38 myeloproliferative neoplasms 38 metabolic disorder 38 super spreaders 38 aristocratic 38 lactose malabsorption 38 kidney disease 38 causative gene 38 Nasal allergies 38 dukedom 38 inherited degenerative 38 autism dyslexia 38 ASD autism spectrum 38 childhood disintegrative disorder 38 Phenylketonuria 38 undiagnosed congenital