Related by context. All words. (Click for frequent words.) 68 metabolic disorder 67 phenylketonuria 67 degenerative disorder 66 genetic disorder 65 blood clotting disorder 64 genetic defect 64 neurodegenerative disorder 64 hereditary disorder 64 brain malformation 64 chronic granulomatous disease 64 autoimmune disorder 63 xeroderma pigmentosum 63 Pompe Disease 62 Joubert syndrome 62 ADPKD 62 congenital disorder 62 Leber congenital amaurosis 62 Leber congenital amaurosis LCA 62 AAT deficiency 62 Hurler syndrome 61 autosomal recessive disorder 61 Coeliac disease 61 lysosomal storage disease 61 Fanconi anemia 61 Sanfilippo syndrome 61 myotonic dystrophy 61 Hurler Syndrome 61 iron overload 61 Hashimoto thyroiditis 61 chromosomal defect 61 Sanfilippo Syndrome 61 NAGS deficiency 61 lysosomal storage diseases 60 autoimmune disease 60 fatal neurodegenerative 60 Lafora disease 60 Pulmonary hypertension 60 genetic lysosomal storage 60 chromosomal disorder 60 dyskeratosis congenita 60 BH4 deficiency 60 Hypophosphatasia 60 lysosomal diseases 60 RPE# 60 lactase deficiency 60 Niemann Pick disease 60 Cockayne syndrome 60 fatal neurodegenerative disorder 60 anemias 60 monogenic 60 Cockayne Syndrome 60 Hereditary angioedema HAE 60 glomerulonephritis 60 nerve degeneration 60 hyperparathyroidism 59 hemochromatosis 59 Von Willebrand disease 59 progressive degeneration 59 Leber Congenital Amaurosis LCA 59 recessive dystrophic epidermolysis bullosa 59 inherited neurological disorder 59 genetic syndromes 59 myopathies 59 progressive neurodegenerative disorder 59 epidermolysis bullosa 59 myasthenia gravis MG 59 medium chain acyl 59 chromosome abnormality 59 leukoencephalopathy 59 clotting disorder 59 atypical hemolytic uremic syndrome 59 gastrointestinal stromal tumor 59 cystic fibrosis chronic pancreatitis 59 Iron deficiency anemia 59 liver scarring 59 familial hypercholesterolemia 59 SMN protein 59 autosomal dominant 59 Anencephaly 59 neuropsychiatric disorder 59 spinal muscular atrophy SMA 59 glucocerebroside 59 inherited retinal degeneration 59 holoprosencephaly 59 epidermolysis bullosa EB 58 autoinflammatory diseases 58 mastocytosis 58 autoimmune hemolytic anemia 58 podocytes 58 Hyperthyroidism 58 Hemolytic Uremic Syndrome HUS 58 cardiac hypertrophy 58 Aplastic anemia 58 Medulloblastoma 58 AAT Deficiency 58 familial adenomatous polyposis 58 biliary atresia 58 genetic mutation 58 Insulin resistance 58 hemolytic anemia 58 Retinitis pigmentosa 58 hormonal disorder 58 Aortic stenosis 58 Diamond Blackfan anemia 58 inherited neurodegenerative 58 Vitamin B# deficiency 58 Krabbe Leukodystrophy 58 incurable genetic 58 multisystem disorder 58 haemolytic anemia 58 Carcinoid tumors 58 untreated celiac disease 58 Leber hereditary optic neuropathy 58 Myopathy 58 Hypothyroidism 58 spinocerebellar ataxia 58 recessive trait 58 septo optic dysplasia 58 Myasthenia gravis 58 NF2 58 genetic abnormality 58 osteogenesis imperfecta 58 metabolic abnormality 58 DiGeorge syndrome 58 Factor XIII 58 static encephalopathy 58 Myotonic dystrophy 58 underactive thyroid gland 58 optic nerve hypoplasia 57 inherited neurodegenerative disorder 57 DiGeorge Syndrome 57 autosomal recessive disease 57 ectodermal dysplasia 57 neuro degenerative disease 57 systemic amyloidosis 57 Lupus nephritis 57 FSGS 57 neurofibromas 57 bone deformities 57 coagulopathy 57 NF1 57 motor neuron diseases 57 polycystic kidneys 57 cardiac fibrosis 57 amino acid tyrosine 57 aldehyde dehydrogenase 57 galactosemia 57 filaggrin 57 Hutchinson Gilford progeria 57 Pre eclampsia 57 mitochondrial disorders 57 discoid lupus 57 autosomal dominant disorder 57 Usher Syndrome 57 degenerative retinal disease 57 retinal dysfunction 57 Cystic fibrosis 57 Brugada Syndrome 57 mitochondrial disease 57 tuberous sclerosis complex 57 Leber Hereditary Optic Neuropathy 57 Gorlin syndrome 57 pseudotumor cerebri 57 homozygous FH 57 nonsense mutation 57 malabsorption 57 lipofuscin 57 fatal neuromuscular disorder 57 myelodysplasia 57 Severe Primary IGFD 57 CHD7 57 Stargardt Macular Dystrophy 57 Hutchinson Gilford Progeria Syndrome 57 Hemochromatosis 57 gene mutation 57 obliterative bronchiolitis 57 PKU genetic 57 Hirschsprung Disease 57 limb deformities 57 spastic diplegia 57 neuroblastoma tumor 57 incurable neurodegenerative disease 57 epigenetic alterations 57 thyroid deficiency 57 degenerative neurological disorder 57 hepatic cirrhosis 56 mitochondrial dysfunction 56 dominantly inherited 56 restrictive cardiomyopathy 56 dilated cardiomyopathy 56 Maroteaux Lamy syndrome 56 pernicious anemia 56 Psoriatic arthritis 56 ANCA associated 56 primary biliary cirrhosis 56 uremia 56 neurofibromatosis 56 leukodystrophy 56 neurodevelopmental disorder 56 ependymoma 56 inherited mutations 56 chronic autoimmune disorder 56 hyperinsulinism 56 Myocarditis 56 retinitis pigmentosa RP 56 Retinoblastoma 56 pyloric stenosis 56 nephrotic syndrome 56 Alu RNA 56 Angelman syndrome 56 severe congenital neutropenia 56 spastic paraplegia 56 multisystem disease 56 lactose malabsorption 56 defective gene 56 JMML 56 Ankylosing spondylitis 56 skeletal fluorosis 56 post transplant lymphoproliferative 56 Ehlers Danlos syndrome 56 haemochromatosis 56 Kufs disease 56 variable immunodeficiency 56 Friedreich ataxia 56 recessive genetic 56 hydrops 56 mucus glands 56 Endometrial cancer 56 wet macular degeneration 56 lymphocytic leukemia 56 valvular heart disease 56 paralytic illness 56 von Willebrand disease 56 Alport syndrome 56 autoimmune 56 huntingtin gene 56 pulmonary hypertension PH 56 hereditary spastic paraplegia 56 missense mutation 56 autosomal recessive genetic 56 PTLD 56 ataxia telangiectasia 56 autosomal recessive 56 insulin secreting cells 56 embryonal rhabdomyosarcoma 56 Maroteaux Lamy Syndrome 56 Atopic dermatitis 56 aneuploidies 56 atopic eczema 56 Mitochondrial diseases 56 Ribavirin causes 56 paraneoplastic 56 subependymal giant cell 56 aciduria 56 autosomal dominant polycystic kidney 56 systemic scleroderma 56 epithelial tissues 56 vWD 56 Proteus Syndrome 56 glucocerebrosidase 56 thyroiditis 56 exocrine 56 NADPH oxidase 56 Malignant mesothelioma 56 achalasia 56 Urticaria 56 metabolize cholesterol 56 amino acid phenylalanine 56 Hypertrophic cardiomyopathy 56 folic acid deficiency 56 Diabetic neuropathy 56 Raynaud disease 55 purpura 55 Beta thalassemia 55 juvenile myelomonocytic leukemia 55 eosinophilic 55 atresia 55 choriocarcinoma 55 homocystinuria 55 adenosine deaminase 55 kidney insufficiency 55 urea cycle 55 Male pattern baldness 55 immunodeficiency disorder 55 nonsense mutations 55 beta thalassemia 55 Dravet syndrome 55 tuberous sclerosis 55 leptin deficiency 55 leukemia AML 55 congenital disorders 55 pancreatic endocrine 55 Fabry disease 55 antidiuretic hormone 55 lactase 55 hypocalcaemia 55 NPHP 55 Hirschsprung disease 55 Wilms tumor 55 incurable neurological disorder 55 CHARGE syndrome 55 Fragile X Syndrome 55 Fanconi Anemia 55 autoinflammatory 55 Fibroblasts 55 dystrophy 55 Spinal muscular atrophy 55 goblet cells 55 Diamond Blackfan Anemia 55 progressive retinal degenerative 55 airway constriction 55 Hutchinson Gilford Progeria 55 Eisenmenger syndrome 55 beta globin gene 55 fat malabsorption 55 Henoch purpura 55 epilepsies 55 primary hyperoxaluria 55 mutated protein 55 Gestational diabetes 55 Nephrotic Syndrome 55 hemolytic uremic syndrome HUS 55 hereditary disorders 55 transplanted bone marrow 55 adrenal tumor 55 immunodeficiencies 55 adrenal hormones 55 Niemann Pick 55 rhabdomyosarcoma 55 congenital adrenal hyperplasia CAH 55 Beckwith Wiedemann syndrome 55 muscular dystrophies 55 Lesch Nyhan syndrome 55 Gaucher disease 55 Sjogren Syndrome 55 hematologic disorders 55 Proteus syndrome 55 Hemolytic Uremic Syndrome 55 Duchenne muscular dystrophy DMD 55 Cushing syndrome 55 diabetes insipidus 55 leptin resistance 55 Dilated cardiomyopathy 55 lichen planus 55 Lactose intolerance 55 idiopathic PAH 55 leaky gut 55 Dystrophin 55 FMR1 gene 55 mitochondrial enzyme 55 thrombocytosis 55 eosinophilic esophagitis 55 ADAMTS# 55 blastoma 55 lymphangioleiomyomatosis LAM 55 severe malignant osteopetrosis 55 chronic immune thrombocytopenic 55 exocrine glands 55 hemophagocytic lymphohistiocytosis 55 Thiamine 55 hereditary predisposition 55 Childhood Disorder 55 Meningiomas 55 Krabbe Disease 55 mutated gene 55 Rhabdomyosarcoma 55 Phenylketonuria PKU 55 neurological manifestations 55 Dysplasia 54 Tuberous sclerosis 54 purpura ITP 54 Uveal melanoma 54 Idiopathic pulmonary fibrosis IPF 54 Systemic lupus erythematosus SLE 54 nephrogenic fibrosing dermopathy 54 G6PD deficiency 54 Morquio 54 nephritis 54 Fragile X syndrome 54 arthrogryposis 54 progressive neurodegenerative 54 Hereditary angioedema 54 hyperammonemia 54 enzyme lactase 54 primary pulmonary hypertension 54 neuroblastomas 54 polycystic ovary syndrome 54 Acid reflux 54 Pompe disease rare 54 Becker muscular dystrophy 54 hypophosphatasia 54 progressive degenerative 54 skeletal dysplasia 54 inherited genetic mutation 54 Menkes disease 54 connective tissue disorder 54 Retinopathy 54 congenital blindness 54 BRAF gene 54 Severe Combined Immunodeficiency 54 paroxysmal nocturnal hemoglobinuria 54 genetic neuromuscular disorder 54 MELAS 54 Osteoarthritis OA 54 osteogenesis imperfecta OI 54 hypertrophic cardiomyopathy HCM 54 Osteosarcoma 54 LRAT 54 de novo mutations 54 muscarinic receptors 54 lysosomal storage disorder 54 basal cell nevus syndrome 54 Crouzon syndrome 54 cirrhotic liver 54 interstitial nephritis 54 Pulmonary arterial hypertension 54 pulmonary stenosis 54 Polycystic kidney disease 54 fatty liver disease 54 Obsessive compulsive disorder 54 histiocytosis 54 fronto temporal dementia 54 truncus arteriosus 54 granulomatous 54 transfusion syndrome 54 Angelman Syndrome 54 nutritional deficiency 54 Autoimmune disorders 54 skeletal deformities 54 Acoustic neuromas 54 homozygous familial hypercholesterolemia 54 allergic inflammation 54 Sjögren syndrome 54 Overactive bladder 54 Gastroparesis 54 thoracic aortic aneurysm 54 pancreatitis inflammation 54 fungoides 54 sulfatase 54 dilated cardiomyopathy DCM 54 C1 INH deficiency 54 microangiopathy 54 Myelodysplastic syndrome 54 myotonia 54 arthropathy 54 HbF 54 fibrodysplasia ossificans progressiva 54 mucins 54 achromatopsia 54 bacterial overgrowth 54 Foodborne botulism 54 TPMT 54 blood clotting protein 54 Chronic lymphocytic leukemia CLL 54 mental retardation epilepsy 54 JAK2 enzyme 54 Cystic fibrosis CF 54 molecular abnormalities 54 osteogenic sarcoma 54 dysmotility 54 neurologic disorder 54 toxic megacolon 54 aortic valve stenosis 54 calcium oxalate stones 54 hormone thyroxine 54 leukemias lymphomas 54 sickle hemoglobin 54 dystrophin protein 54 Chronic inflammation 54 beta amyloid accumulation 54 Crohns disease 54 fibrotic disease 54 hormone insulin 54 toxic beta amyloid 54 metabolic acidosis 54 generalized epilepsy 54 neovascularization 54 corneal dystrophy 54 Ectodermal Dysplasia 54 Neovascular Age Related Macular 54 alveolar rhabdomyosarcoma 54 abnormal proteins 54 periventricular leukomalacia 54 plexiform neurofibromas 54 interleukins 54 Primary IGFD 54 Ketoacidosis 54 persistent pulmonary hypertension 54 HLA B# 54 Celiac disease 54 β thalassemia 54 adrenal function 54 neurobehavioral disorder 54 fatty acid oxidation 54 Neurofibromatosis type 54 RDEB 54 BCL#A 54 6 phosphate dehydrogenase 54 neoplastic cells 54 degenerative disorders 54 chromosomal translocation 54 chromosomal abnormality 54 phenylalanine 54 teratoma 54 progressive neurodegenerative disease 54 polymyalgia 54 toxic amyloid beta 54 Krabbe disease 54 Churg Strauss syndrome 54 muscle degeneration 54 enterotoxin 54 mycosis fungoides 54 digestive disorder 54 retinal pigment epithelium 54 cystic lesions 54 Chronic pancreatitis 54 Wet AMD 54 motor neurones 54 acetylcholinesterase 54 Glioblastoma Multiforme GBM 54 intestinal polyps 54 erythropoiesis 54 chiari malformation 54 juvenile dermatomyositis 54 motor neuron degeneration 54 Cardiac hypertrophy 54 protein tau 54 abnormal hemoglobin 54 Peripheral neuropathy 54 Brugada syndrome 54 excitotoxicity 54 yeast overgrowth 54 neuroendocrine cells 54 Raynaud syndrome 53 neurological disorder 53 Oxidative stress 53 calcium oxalate 53 MPGN 53 dystrophies 53 polyneuropathy 53 osteomalacia 53 peroxisomal 53 hyperphosphatemia 53 pancreatic insufficiency 53 achondroplasia 53 Wernicke Korsakoff syndrome 53 heart arrhythmias 53 limb girdle muscular dystrophy 53 polymorphic ventricular tachycardia 53 diffuse intrinsic pontine glioma 53 metabolic disturbances 53 dehydrogenase deficiency 53 hormone glucagon 53 underactive thyroid 53 congenital muscular dystrophy 53 Fibrosis 53 secretes insulin 53 Pompe disease 53 frequent blood transfusions 53 neuronal dysfunction 53 Arrhythmogenic Right Ventricular Cardiomyopathy 53 endocrine gland 53 demyelination 53 rheumatic disease 53 hypertrichosis 53 mitochondrial mutations 53 excess uric acid 53 proteoglycan 53 Acute myeloid leukemia 53 ketone bodies 53 autoimmune thyroiditis 53 1 Antitrypsin Deficiency 53 unknown etiology 53 acute porphyria 53 osteopetrosis 53 Li Fraumeni syndrome 53 degenerative neurological disease 53 NOTCH1 53 lymphoid organs 53 fibrin deposition 53 mitochondrial diseases 53 Chronic lymphocytic leukemia 53 cardiac channelopathies 53 pancytopenia 53 kappa opioid receptors 53 debilitating autoimmune 53 MPS VI 53 Hemophilia B 53 demyelinating disease 53 pancreatic alpha 53 Acidosis 53 intestinal inflammation 53 paraganglioma 53 primary ciliary dyskinesia 53 huntingtin protein 53 hyperalgesia 53 infantile spasms 53 β cells 53 congenital anomaly 53 myxedema 53 congenital deafness 53 Cryptococcus neoformans 53 Hypertrophic 53 Aicardi syndrome 53 Mitral regurgitation 53 Krabbe leukodystrophy 53 Acute pancreatitis 53 Tumor Necrosis Factor 53 overactivation 53 familial ALS 53 HGPS 53 chronic autoimmune 53 secondary hyperparathyroidism 53 IgA deficiency 53 hypereosinophilic syndrome 53 late infantile neuronal 53 neurological disorder affecting 53 enteropathy 53 lactic acidosis 53 polyomavirus nephropathy 53 aplastic anemia 53 infantile onset 53 neurodevelopment disorder 53 Magnesium deficiency 53 myasthenia gravis 53 Obstructive sleep apnea 53 cardiomyopathy weakening 53 celiac sprue 53 acute GvHD 53 Diabetic retinopathy 53 Cancer cachexia 53 hypercalciuria 53 Sandhoff disease 53 endocrine disorder 53 debilitating complication 53 iritis 53 progressive neurologic 53 parathyroid gland 53 calcium deficiency 53 dystrophin gene 53 medulloblastoma tumors 53 Malassezia 53 Morquio syndrome 53 thrombotic thrombocytopenic purpura 53 rheumatoid arthritis lupus 53 idiopathic 53 ATTR PN 53 cerebri 53 Gliomas 53 Tay Sachs disease 53 Zollinger Ellison syndrome 53 abnormal lymphocytes 53 oral thrush 53 Glioma 53 Angiotensin II 53 optic neuropathy 53 Barrett esophagus precancerous 53 Muscular dystrophy 53 fibromatosis 53 Peutz Jeghers syndrome 53 mitral valve regurgitation 53 galactose intolerance severe 53 Ulcerative colitis 53 disease NAFLD 53 Diabetic nephropathy 53 Uncontrolled diabetes 53 hereditary deafness 53 acute promyelocytic leukemia 53 familial hypercholesterolemia FH 53 vWF 53 glial derived neurotrophic 53 Fas ligand 53 MECP2 gene 53 Cholangiocarcinoma 53 gluten protein 53 FTLD 53 Seborrheic dermatitis 53 Zinc deficiency 53 Leukemias 53 porphyria 53 Neural stem cells 53 rare neurological disorder 53 disseminated intravascular coagulation 53 Periodontal disease 53 hemolytic 53 BCR ABL protein 53 epiglottitis 53 lissencephaly 53 mesangial 53 mesothelial cells 53 Cerebral malaria 53 multiorgan 53 recurrent infections 53 Rett syndrome 53 steatohepatitis 53 prematurity ROP 53 malformation 53 myeloproliferative disease 53 fibrogenesis 53 lymphocytic 53 cystine 53 disorder thalassemia 53 Temporal lobe epilepsy 53 immunodeficiency 53 oligodendrocyte progenitor cells 53 Progeria 53 SMN2 53 Systemic lupus erythematosus 53 CFTR gene 53 Aortic dissection 53 oxalate 53 nonalcoholic steatohepatitis NASH 53 activin 53 spinal muscular atrophy 53 ADA SCID 53 developmental abnormalities 53 hemangioma 52 familial adenomatous polyposis FAP 52 insulin hormone secreted 52 uric acid 52 arthritis RA 52 amyloid deposits 52 virally induced 52 chromosomal anomaly 52 Crouzon Syndrome 52 Congestive heart failure 52 acidosis 52 neurofibroma 52 IRS1 52 chronic eosinophilic leukemia 52 otitis 52 Fibrous Dysplasia 52 TSLP 52 torsade de pointes 52 retinal dystrophy 52 myoclonic epilepsy 52 PARP inhibition 52 glutamic acid decarboxylase 52 CYP #A# 52 intractable epilepsy 52 nephrosis 52 lymphoblasts 52 AA amyloidosis 52 primary sclerosing cholangitis 52 neuroendocrine tumors 52 fructose intolerance 52 1 antitrypsin 52 Rhabdomyolysis 52 myelopathy 52 glycogen storage 52 bullous pemphigoid 52 Shwachman Diamond Syndrome 52 mutant huntingtin protein 52 Thyroid hormone 52 myelodysplastic syndrome MDS 52 vasculitis 52 corneal scarring 52 idiopathic thrombocytopenic purpura ITP 52 chronic acid reflux 52 angiosarcoma 52 Alzheimer Disease AD 52 glycated 52 Moyamoya disease 52 amyloid proteins 52 juvenile idiopathic arthritis JIA 52 Parkinson degenerative 52 bone marrow suppression 52 Esophagitis 52 medulloblastoma 52 retinal degeneration 52 Acute Myeloid Leukaemia 52 insulin resistance syndrome 52 JAK mutations 52 ceroid lipofuscinosis NCL 52 hereditary blindness 52 hyperplasia 52 irreversible blindness 52 lung fibrosis 52 adrenal cortex 52 Genetic mutations 52 atherosclerotic lesions 52 nephron 52 parathyroid glands 52 unprovoked seizures 52 Interstitial cystitis 52 recurrent seizures 52 Meckel Gruber syndrome 52 bullous 52 Wiskott Aldrich Syndrome 52 hereditary hemorrhagic telangiectasia 52 IRAK1 52 enterocolitis 52 Polycystic ovary syndrome PCOS 52 hereditary degenerative 52 SOD2 gene 52 idiopathic thrombocytopenic purpura 52 Polymorphic Ventricular Tachycardia CPVT 52 metachromatic leukodystrophy 52 congenital diaphragmatic hernia 52 pigmentosa 52 pancreatic enzymes 52 SMN1 52 LDL receptor 52 thyrotoxicosis 52 pancreas 52 Six3 52 neurological degeneration 52 Acromegaly 52 Host Disease GvHD 52 hyperkalemia 52 SSc 52 Noonan Syndrome 52 neuro developmental disorder 52 T1DM 52 Stargardt Disease 52 phenylketonuria PKU 52 Bardet Biedl syndrome 52 alpha1 antitrypsin deficiency 52 TTR amyloidosis 52 cirrhosis liver failure 52 debilitating neurodegenerative disorder 52 progressive neuromuscular 52 scleroderma chronic 52 neurofibrillary 52 Genetic mutation 52 secrete insulin 52 enzyme glucocerebrosidase 52 Sjogren syndrome 52 survival motor neuron 52 generalized seizures 52 fatal neurological disorder 52 protein misfolding 52 Atopic eczema 52 hereditary hemochromatosis 52 Chiari malformation 52 progressive neurodegenerative disorders 52 giant cell arteritis 52 BH4 52 melanin pigment 52 Cyclin D1 52 tricuspid atresia 52 Idiopathic Thrombocytopenic Purpura 52 pancreas pancreatitis 52 Diverticulosis 52 Pervasive Developmental Disorder 52 electrolyte imbalances 52 gluconeogenesis 52 childhood disintegrative disorder 52 orchitis 52 crystallin 52 Familial Adenomatous Polyposis FAP 52 Prader Willi syndrome 52 Holoprosencephaly 52 intestinal epithelium 52 1 diabetes T1D 52 skeletal malformations 52 molybdenum cofactor deficiency 52 behavioral abnormalities 52 cholestasis 52 Selenium deficiency 52 glucosylceramide 52 Sclerosing 52 dysplasia 52 diseases chronic granulomatous 52 ichthyosis vulgaris 52 beta adrenergic receptors 52 channelopathies 52 nonalcoholic cirrhosis 52 Hyperplasia 52 overactive thyroid gland 52 antithrombin deficiency 52 thyroid hormone deficiency 52 MODY 52 pheochromocytoma 52 hematological diseases 52 dysgenesis 52 hypothyroidism 52 carcinoid tumors 52 Critical limb ischemia 52 Pericarditis 52 hypoplasia 52 undergo apoptosis 52 axonal damage 52 acidemia 52 cardiac fibroblasts 52 beta amyloid peptide 52 WAGR syndrome 52 inherited metabolic disorders 52 pancreatic tissue 52 hyperphenylalaninemia HPA due 52 amyloidosis 52 inhibit enzymes 52 Idiopathic pulmonary fibrosis 52 microvascular dysfunction 52 autoimmune disorder characterized 52 Fatty liver 52 suppurative 52 ketoacidosis 52 mutant protein 52 polydactylism 52 #beta HSD1 52 kidney dysfunction 52 elastic fibers 52 haemolysis 52 lipid synthesis 52 aplasia 52 polycystic kidney disease 52 esophageal atresia 52 Osteogenesis imperfecta 52 dysplasias 52 PGC 1α 52 Oppositional Defiant Disorder 52 optic atrophy 52 Uric acid 52 degenerative retinal diseases 52 RPE# gene 52 GISTs 52 nicotinamide 52 Degenerative disc disease 52 Bcr Abl 52 ductal adenocarcinoma 52 MTHFR 52 hyperplastic 52 degenerative neurological diseases 52 ataxias 52 Cysts 52 Systemic lupus 52 intracranial hemorrhage ICH 52 C1q 52 Mucositis 52 involuntary tics 52 1 antitrypsin deficiency 52 blastic 52 Iron deficiency 52 seborrhea 52 Malformation 52 podocyte 52 pituitary tumors 52 amyloid β 52 Lennox Gastaut syndrome 52 receptor subtype 52 Epstein Barr Virus EBV 52 necrotising 52 leukaemias 52 congenital abnormality 52 severe aplastic anemia 52 thrombocytopenia neutropenia 52 MCAD deficiency 52 progressive neurological disorder 52 Gaucher Disease 52 DGAT1 52 Epstein Barr Virus 52 Long QT Syndrome 52 neurobiological disorder 52 protein dystrophin 52 chitinase 52 Mesenchymal 52 Friedreich Ataxia FRDA 52 digest gluten 52 fluid overload 52 cortical dysplasia 51 cardiac insufficiency 51 spinocerebellar ataxia type 51 potassium deficiency 51 HMGA2 51 Gluten intolerance 51 Leber Congenital Amaurosis 51 hepatorenal syndrome 51 pathologic myopia 51 interstitial pneumonitis 51 tau proteins 51 Aviptadil 51 Mitochondrial 51 Melasma 51 IgA nephropathy 51 multidrug resistance 51 overactivity 51 hyperthyroidism 51 superoxide dismutase 51 infection progressive multifocal 51 arrythmias 51 anemia 51 proliferative diabetic retinopathy 51 juvenile myoclonic epilepsy 51 cystic acne 51 peroxisome 51 Spasticity 51 retinoblastoma 51 Candidiasis 51 leukemia ALL 51 cryptogenic 51 hypercalcemia 51 Colorectal cancers 51 microdeletion 51 Hemangiomas 51 neovascularisation 51 MCADD 51 Bullous 51 myositis