Related by context. All words. (Click for frequent words.) 69 genetic disorder 69 degenerative disorder 67 neurodegenerative disorder 66 fatal neurodegenerative 66 fatal neurodegenerative disorder 65 Hereditary angioedema HAE 65 metabolic disorder 65 genetic defect 64 enzyme deficiency 64 chromosomal defect 64 chronic granulomatous disease 64 inherited neurological disorder 64 neuro degenerative disease 64 Joubert syndrome 64 chromosome abnormality 64 inherited neurodegenerative disorder 64 progressive neurodegenerative disorder 63 inherited neurodegenerative 63 congenital disorder 63 genetic abnormality 63 Retinitis pigmentosa 63 Aplastic anemia 63 ataxia telangiectasia 62 multisystem disease 62 chromosomal disorder 62 blood clotting disorder 62 Aortic stenosis 62 Brugada Syndrome 62 autosomal dominant 62 Maroteaux Lamy syndrome 62 Dravet syndrome 61 epidermolysis bullosa EB 61 Hutchinson Gilford Progeria Syndrome 61 autosomal dominant disorder 61 Usher Syndrome 61 Krabbe Disease 61 Krabbe Leukodystrophy 61 Cystic fibrosis CF 61 dominantly inherited 61 septo optic dysplasia 61 Pulmonary hypertension 61 Cholangiocarcinoma 61 Noonan Syndrome 61 AAT deficiency 61 CHARGE syndrome 61 myotonic dystrophy 61 Leber congenital amaurosis LCA 61 spinal muscular atrophy SMA 61 progressive neurodegenerative 61 progressive degeneration 61 degenerative neurological disease 60 Spinal muscular atrophy 60 autosomal recessive disease 60 Coeliac disease 60 Pulmonary arterial hypertension 60 Cystic fibrosis 60 hypophosphatasia 60 progressive neurodegenerative disease 60 neuropsychiatric disorder 60 AAT Deficiency 60 progressive neurological disorder 60 Fragile X Syndrome 60 autosomal recessive disorder 60 congenital deafness 60 Cockayne syndrome 60 paralytic illness 60 brain malformation 60 Retinopathy 60 Hurler syndrome 60 holoprosencephaly 60 ectodermal dysplasia 60 Pompe Disease 60 severe malignant osteopetrosis 60 fatal neuromuscular disorder 59 medium chain acyl 59 Leber congenital amaurosis 59 Long QT Syndrome 59 nonsense mutation 59 Tuberous sclerosis 59 multisystem disorder 59 gene mutation 59 disabling neurological 59 degenerative neurological disorder 59 Myasthenia gravis 59 spinal muscle atrophy 59 Von Willebrand disease 59 debilitating autoimmune 59 recessive genetic 59 autosomal recessive 59 progressive degenerative 59 Leber hereditary optic neuropathy 59 dyskeratosis congenita 59 genetic mutation 58 hydrops 58 Retinoblastoma 58 galactosemia 58 Angelman syndrome 58 Hirschsprung disease 58 chronic autoimmune disorder 58 Niemann Pick disease 58 hemophagocytic lymphohistiocytosis 58 Kufs disease 58 autosomal recessive genetic 58 Maroteaux Lamy Syndrome 58 biliary atresia 58 Hypophosphatasia 58 MELAS 58 leukodystrophy 58 optic nerve hypoplasia 58 motor neuron diseases 58 beta thalassemia 58 defective gene 58 Fragile X syndrome 58 neurodevelopmental disorder 58 incurable neurodegenerative disease 58 prematurity ROP 58 genetic neuromuscular disorder 58 retinitis pigmentosa RP 58 achromatopsia 58 blastoma 58 Tay Sachs disease 58 arrhythmogenic right 58 neurological disorder 58 Polycystic kidney disease 58 familial adenomatous polyposis 58 spinocerebellar ataxia 58 Fanconi anemia 58 Medulloblastoma 58 ATTR PN 58 autoimmune thyroiditis 58 degenerative nerve disease 58 lysosomal storage disease 57 Leber Congenital Amaurosis LCA 57 RPE# 57 congenital diaphragmatic hernia 57 huntingtin gene 57 pseudotumor cerebri 57 Hurler Syndrome 57 Friedreich ataxia 57 blood clotting disorders 57 nephritis 57 Alport Syndrome 57 diseases chronic granulomatous 57 NF1 57 LQTS 57 ADPKD 57 retinal degeneration 57 juvenile myelomonocytic leukemia 57 Parkinson degenerative 57 Systemic lupus erythematosus SLE 57 Arrhythmogenic Right Ventricular Cardiomyopathy 57 inherited mutations 57 chromosomal abnormality 57 autoimmune disorder 57 retinal dysfunction 57 Retinitis Pigmentosa RP 57 Eisenmenger syndrome 57 recessive dystrophic epidermolysis bullosa 57 genetic disorders 57 hereditary degenerative 57 Duchenne muscular dystrophy DMD 57 Diabetic retinopathy 57 Myotonic dystrophy 57 homozygous familial hypercholesterolemia 57 Krabbe leukodystrophy 57 inherited retinal degeneration 57 Peutz Jeghers syndrome 57 congenital anomaly 57 Parkinson disease neurodegenerative disorder 57 immunodeficiency disorder 57 Sanfilippo Syndrome 57 genetically inherited 57 fatal myelination disorder 57 Nephrotic Syndrome 57 phenylketonuria 57 1 Antitrypsin Deficiency 57 cardiac hypertrophy 57 pigmentosa 56 Prader Willi syndrome 56 Spina bifida 56 hemolytic anemia 56 Becker muscular dystrophy 56 neurological disorder affecting 56 neurodegenerative disease 56 enterocolitis 56 nerve degeneration 56 ceroid lipofuscinosis NCL 56 Autoimmune disorders 56 DiGeorge syndrome rare 56 Endometrial cancer 56 leukoencephalopathy 56 autoimmune disease 56 Cockayne Syndrome 56 tuberous sclerosis complex 56 Aortic dissection 56 osteogenesis imperfecta 56 epidermolysis bullosa 56 Long QT syndrome 56 hormonal disorder 56 polymorphic ventricular tachycardia 56 Treacher Collins syndrome 56 genetic lysosomal storage 56 lysosomal storage diseases 56 DiGeorge syndrome 56 primary pulmonary hypertension 56 regulator CFTR gene 56 dysgenesis 56 Muscular dystrophy 56 Mitochondrial diseases 56 xeroderma pigmentosum 56 Anencephaly 56 primary ciliary dyskinesia 56 optic atrophy 56 neuro developmental disorder 56 leukodystrophies 56 tics involuntary 56 muscle degeneration 56 Churg Strauss syndrome 56 Rett syndrome 56 Ehlers Danlos syndrome 56 Crouzon Syndrome 56 Pompe disease rare 56 genetic defects 56 Pelizaeus Merzbacher disease 56 cerebellar ataxia 56 incurable neurological disorder 56 filaggrin 56 Parkinson disease degenerative 56 chronic neurological disorder 56 Iron deficiency anemia 56 Lafora disease 56 DiGeorge Syndrome 56 optic neuropathy 56 Brugada syndrome 56 motor neuron degeneration 56 dilated cardiomyopathy 56 recurrent seizures 56 Hirschsprung Disease 56 Critical limb ischemia 56 glomerulonephritis 56 Proteus syndrome 56 thyroiditis 56 Diabetic neuropathy 56 lysosomal diseases 56 Hemochromatosis 56 congenital abnormality 56 demyelinating disease 56 degenerative nerve disorder 56 variable immunodeficiency 56 Marfan Syndrome 56 Multiple sclerosis MS 56 infection progressive multifocal 55 clotting disorder 55 Cryptococcus neoformans 55 Tetralogy 55 Pulmonary fibrosis 55 lysosomal storage disorder 55 G#S mutation 55 Osteosarcoma 55 Cardiomyopathy 55 NF2 55 Beckwith Wiedemann Syndrome 55 G6PD deficiency 55 osteopetrosis 55 Jakob Disease 55 Beta thalassemia 55 auditory neuropathy 55 PKU genetic 55 Krabbe disease 55 systemic scleroderma 55 Chronic lymphocytic leukemia 55 debilitating neurological disorder 55 congenital adrenal hyperplasia CAH 55 Acute myeloid leukemia 55 achondroplasia 55 Down syndrome chromosomal disorder 55 Li Fraumeni syndrome 55 Hereditary angioedema 55 degenerative neurological condition 55 hereditary deafness 55 Chiari malformation 55 long QT syndrome 55 Motor neurone disease 55 gastrointestinal stromal tumor 55 Proteus Syndrome 55 Alport syndrome 55 incurable genetic 55 Aicardi syndrome 55 myelodysplasia 55 Rheumatic fever 55 Fatty liver 55 neurological disorder characterized 55 disease NAFLD 55 Ulcerative colitis 55 aortic valve stenosis 55 Sickle cell 55 Peanut allergy 55 degenerative disorders 55 spastic diplegia 55 Stargardt Macular Dystrophy 55 Von Hippel Lindau 55 HGPS 55 Fibrous Dysplasia 55 chronic autoimmune 55 neuroblastoma tumor 55 Duchenne Muscular Dystrophy DMD 55 Stargardt Disease 55 Lactose intolerance 55 sacral agenesis 55 Malignant mesothelioma 55 dysmotility 55 eosinophilic esophagitis 55 hematologic disorders 55 Oral mucositis 55 polycystic kidneys 55 lymphangioleiomyomatosis LAM 55 mastocytosis 55 leukoencephalopathy PML 55 neural tube defect 55 neuro degenerative 55 truncus arteriosus 55 Hypertrophic cardiomyopathy 55 Leber Hereditary Optic Neuropathy 55 SCN5A 55 von Willebrand disease 55 Atopic dermatitis 55 myasthenia gravis MG 55 ataxia telangiectasia AT 55 primary sclerosing cholangitis 55 Congenital Adrenal Hyperplasia 55 neurobehavioral disorder 55 Myopathy 55 metachromatic leukodystrophy 55 Angelman Syndrome 55 CFTR gene 55 bicuspid valve 54 Fanconi Anemia 54 Hemophilia B 54 neurodevelopment disorder 54 Hashimoto thyroiditis 54 malformation 54 Magnesium deficiency 54 Obsessive compulsive disorder 54 Obstructive sleep apnea 54 familial hypercholesterolemia 54 ventricular dysplasia 54 amyloidosis 54 Meckel Gruber syndrome 54 hypertrophic cardiomyopathy HCM 54 developmental disorder 54 Apert syndrome 54 vWD 54 retinitis pigmentosa degenerative 54 MPS VI 54 Foodborne botulism 54 irreversible blindness 54 Rubinstein Taybi syndrome 54 discoid lupus 54 obliterative bronchiolitis 54 Obstructive sleep apnea OSA 54 unprovoked seizures 54 hereditary hemochromatosis 54 thyroid deficiency 54 sporadic ALS 54 Usher syndrome 54 progressive neurologic 54 cause cardiac channelopathies 54 CHD7 54 Stargardt disease 54 neuronal degeneration 54 Holoprosencephaly 54 Sjögren syndrome 54 progressive neurodegenerative disorders 54 Atrial fibrillation AF 54 fronto temporal dementia 54 IgA deficiency 54 pyloric stenosis 54 PTLD 54 osteogenesis imperfecta OI 54 degenerative neuromuscular disease 54 cortical dysplasia 54 Canavan Disease 54 MCAD deficiency 54 Meckel Gruber 54 lissencephaly 54 polycystic kidney disease 54 Dilated cardiomyopathy 54 arthrogryposis 54 Combined Immune Deficiency 54 myeloproliferative neoplasms 54 Cerebral palsy 54 heart syndrome HLHS 54 metabolic abnormality 54 neurologic disorder 54 tricuspid atresia 54 degenerative neurological diseases 54 Hutchinson Gilford progeria 54 erythematosus 54 iron overload 54 progressive neuromuscular 54 Macular degeneration 54 adrenoleukodystrophy ALD 54 Essential tremor 54 chiari malformation 54 DISC1 gene 54 endocrine disorder 54 spastic paraplegia 54 medulloblastoma tumors 54 chromosomal anomaly 54 retinitis 54 Duchene muscular dystrophy 54 conjoined twin births 54 Hutchinson Gilford Progeria 54 Hyperthyroidism 54 fungal meningitis 54 Morquio syndrome 54 Gastroparesis 54 Male pattern baldness 54 myelomeningocele 54 Diamond Blackfan anemia 54 paraneoplastic 54 muscular dystrophies 54 epilepsies 54 myalgic encephalomyelitis ME 54 esophageal atresia 54 NAGS deficiency 54 Rhabdomyosarcoma 54 cystic fibrosis Duchenne muscular 54 myelopathy 54 Mitochondrial disease 54 Klippel Trenaunay Syndrome 54 MELAS syndrome 54 neuromuscular disorder 54 hyperparathyroidism 54 pulmonary atresia 54 hereditary disorders 54 fibrotic disease 54 autoinflammatory diseases 54 progeria rare 54 mitochondrial disease 54 Raynaud disease 54 Bardet Biedl syndrome 53 dystrophy 53 Idiopathic pulmonary fibrosis IPF 53 Hypothyroidism 53 Alagille syndrome 53 mutated gene 53 Major depressive disorder 53 non alcoholic steatohepatitis 53 Hypoplastic Left Heart 53 myopathies 53 autosomal dominant polycystic kidney 53 cystic fibrosis chronic pancreatitis 53 Insulin resistance 53 humans variant Creutzfeldt 53 Malignant glioma 53 neurological ailment 53 syringomyelia 53 immunodeficiencies 53 Basal cell carcinoma 53 congenital disorders 53 Niemann Pick 53 paraganglioma 53 CIDP 53 neuro degenerative disorder 53 Ectodermal Dysplasia 53 nonalcoholic cirrhosis 53 Polymorphic Ventricular Tachycardia CPVT 53 persistent pulmonary hypertension 53 degenerative disease 53 Leukodystrophy 53 idiopathic thrombocytopenic purpura 53 Idiopathic pulmonary fibrosis 53 Severe Combined Immunodeficiency 53 Glioma 53 ARVD 53 neurodegenerative disorder characterized 53 intestinal inflammation 53 Polycystic Kidney Disease 53 heart arrhythmias 53 osteogenic sarcoma 53 chronic degenerative 53 post transplant lymphoproliferative 53 Mucositis 53 idiopathic 53 static encephalopathy 53 monogenic 53 Dystrophin 53 Sturge Weber syndrome 53 Spinal Muscular Atrophy SMA 53 Amyotrophic lateral sclerosis 53 Tay Sachs thalassemia 53 atresia 53 Hip dysplasia 53 Overactive bladder 53 Wilms tumor 53 TTR amyloidosis 53 Marfan syndrome 53 neurological dysfunction 53 Burkitt lymphoma 53 motor neuron disease 53 paroxysmal nocturnal hemoglobinuria 53 Polycystic ovary syndrome PCOS 53 anencephaly 53 Peripheral neuropathy 53 Perthes disease 53 haemolytic anemia 53 hypothalamic hamartoma 53 systemic amyloidosis 53 idiopathic generalized epilepsy 53 Vitamin B# deficiency 53 neovascularisation 53 Ribavirin causes 53 mutation 53 amniotic fluid embolism 53 Wilm Tumor 53 Glioblastoma 53 lactase deficiency 53 neurofibromatosis 53 Psoriatic arthritis 53 1 antitrypsin deficiency 53 mental retardation cerebral palsy 53 Hemolytic Uremic Syndrome 53 hemochromatosis 53 debilitating complication 53 neural tube defects NTDs 53 Tourette syndrome neurological disorder 53 rheumatic disease 53 neurological degeneration 53 late infantile neuronal 53 Ataxia Telangiectasia 53 Ankylosing spondylitis 53 Crohn disease chronic 53 1 antitrypsin 53 recessive trait 53 Glioblastoma multiforme GBM 53 Lupus nephritis 53 Systemic lupus erythematosus 53 neurological complications 53 homozygous FH 53 Peripheral arterial disease 53 Peritoneal mesothelioma 53 torsade de pointes 53 Sarcoidosis 53 de novo mutations 53 anemias 53 retinal degenerative disease 53 Sanfilippo syndrome 53 SMN protein 53 combined immunodeficiency SCID 53 genetic abnormalities 53 severe congenital neutropenia 53 urogenital chlamydiosis 53 autoimmune hemolytic anemia 53 1 diabetes T1D 53 Severe Primary IGFD 53 Sandhoff disease 53 nonhereditary 53 birth defect 53 Parkinson disease neurological disorder 53 HNPCC 53 Colorectal cancers 53 Myelodysplastic syndrome 53 Arnold Chiari Malformation 53 Genital herpes 53 BH4 deficiency 53 limb deformities 53 polyneuropathy 53 Nephrogenic Systemic Fibrosis NSF 53 neurological manifestations 53 MODY 53 skeletal dysplasia 53 cardiac channelopathies 53 Histiocytosis 53 neuromuscular disease 53 congenital hypothyroidism 53 disorder thalassemia 53 chronic eosinophilic leukemia 53 Preeclampsia 52 Gestational diabetes 52 Dysplasia 52 Peripheral artery disease 52 muscular degeneration 52 retinitis pigmentosa 52 familial dysautonomia 52 Diffuse Intrinsic Pontine Glioma 52 Beckwith Wiedemann syndrome 52 Carcinoid tumors 52 familial hypercholesterolemia FH 52 sporadic Creutzfeldt Jakob 52 PAOD 52 Fanconi anemia FA 52 lymphocytic leukemia 52 Fibrosis 52 mitochondrial dysfunction 52 Morquio 52 phonic tics 52 rhabdomyosarcoma 52 Testicular cancer 52 hereditary hemorrhagic telangiectasia 52 Von Willebrand 52 DIPG 52 primary IGFD 52 6 phosphate dehydrogenase 52 Klinefelter syndrome 52 disease CJD 52 diffuse intrinsic pontine glioma 52 Factor XIII 52 Chronic lymphocytic leukemia CLL 52 aciduria 52 hereditary predisposition 52 Prion diseases 52 Glioblastoma multiforme 52 FMRP protein 52 autoimmune encephalitis 52 Pre eclampsia 52 CDH1 52 ependymoma 52 Congestive heart failure 52 Cerebral malaria 52 dermopathy 52 spastic paralysis 52 inflammatory demyelinating 52 Chronic Inflammatory Demyelinating Polyneuropathy 52 genetic syndromes 52 Sensorineural hearing loss 52 neuronal ceroid lipofuscinosis NCL 52 spastic cerebral palsy 52 severe aplastic anemia 52 embryonal rhabdomyosarcoma 52 neurofibroma 52 inherited metabolic disorders 52 NPHP 52 neurobiological disorder 52 Friedreich Ataxia 52 complement inhibitor eculizumab 52 lichen planus 52 Parkinsons disease 52 Thrombocytopenia 52 Lesch Nyhan syndrome 52 Sporadic CJD 52 Idiopathic Thrombocytopenic Purpura ITP 52 spinocerebellar ataxia type 52 severe dehydrating diarrhea 52 bone deformities 52 acromegaly 52 subependymal giant cell 52 polycystic ovarian syndrome PCOS 52 RDEB 52 Fabry disease 52 alveolar rhabdomyosarcoma 52 untreated celiac disease 52 chorea associated 52 cholestasis 52 inherited genetic mutations 52 leptin deficiency 52 autoimmune disorder characterized 52 pulmonary stenosis 52 Epstein Barr virus EBV 52 aortic rupture 52 diabetes mellitus T2DM 52 bacterium Neisseria meningitidis 52 Neurofibromatosis 52 Acute Myelogenous Leukemia 52 Cushing syndrome 52 Wilms Tumor 52 gene MECP2 52 myelogenous leukemia 52 disorder characterized 52 congenital deficiency 52 causative gene 52 G#S [002] 52 ANCA associated 52 fungoides 52 muscular dystrophy cystic fibrosis 52 Myelodysplastic syndromes 52 developmental abnormalities 52 Vitamin D insufficiency 52 MCADD 52 Xeroderma Pigmentosum XP 52 childhood disintegrative disorder 52 insulin resistance syndrome 52 skeletal malformations 52 defects CHDs 52 Neurofibromatosis type 52 Huntingtons disease 52 syndrome FAS 52 renal fibrosis 52 congenital muscular dystrophy 52 Chronic ITP 52 Pulmonary embolism 52 FMR1 gene 52 transfusion syndrome 52 Amyotrophic lateral sclerosis ALS 52 FSGS 52 Seborrheic dermatitis 52 Langerhans cell histiocytosis 52 arterial calcification 52 Celiac disease 52 progressive degenerative neurological 52 thrombotic thrombocytopenic purpura 52 cystic fibrosis CF 52 inherited degenerative 52 JMML 52 Henoch purpura 52 Epidermolysis bullosa 52 Wiskott Aldrich Syndrome 52 involuntary movements 52 atypical hemolytic uremic syndrome 52 Neurofibromatosis Type 52 parasite Trypanosoma cruzi 52 lupus erythematosus 52 myasthenia gravis 52 mitochondrial disorders 52 bronchopulmonary dysplasia 52 Necrotizing fasciitis 52 Shwachman Diamond Syndrome 52 disorder 52 Selenium deficiency 52 MPGN 52 inherited retinal 52 pernicious anemia 52 Dwarfism 52 lateral sclerosis 52 carcinoid 52 hereditary spastic paraplegia 51 epiglottitis 51 Arteriovenous Malformation 51 capillary leak 51 Apert Syndrome 51 phenylketonuria PKU 51 rare autosomal recessive 51 optic neuropathy NAION 51 Moyamoya disease 51 ataxias 51 Menkes disease 51 Tourette Syndrome TS 51 Huntington Chorea 51 Atrial fibrillation 51 hereditary blindness 51 prion disease 51 cystic fibrosis transmembrane conductance 51 myelodysplastic syndrome 51 Periodontal disease 51 thyroid dysfunction 51 nonsense mutations 51 immunodeficiency 51 Chiari Malformation 51 supraventricular tachycardia 51 primary ovarian insufficiency 51 Malignant hyperthermia 51 necrotizing enterocolitis NEC 51 Degenerative disc disease 51 progressive retinal degenerative 51 Prematurity ROP 51 intractable epilepsy 51 epilepsy 51 precocious puberty 51 polyneuropathy CIDP 51 familial ALS 51 intraventricular hemorrhage 51 fibrous dysplasia 51 systemic autoimmune 51 osteosarcoma bone 51 congenital glaucoma 51 Wolf Hirschhorn 51 interstitial lung disease 51 infantile spasms 51 familial adenomatous polyposis FAP 51 Myocarditis 51 Wilm tumor 51 WAGR syndrome 51 Huntington chorea 51 aneuploidies 51 sclerosis ALS 51 aniridia 51 syndrome FXTAS 51 primary hyperoxaluria 51 cystic fibrosis muscular dystrophy 51 spinal muscular atrophy 51 Pompe disease 51 cerebri 51 rare chromosomal disorder 51 parathyroid carcinoma 51 Hemolytic Uremic Syndrome HUS 51 sickle cell cystic fibrosis 51 Acute Myeloid Leukaemia 51 pancytopenia 51 sulfatase 51 Eosinophilic 51 polydactylism 51 Avascular necrosis 51 fatal neuromuscular 51 Langerhans Cell Histiocytosis 51 FMR1 51 Tay Sachs Disease 51 paralysis blindness 51 Gaucher disease 51 non syndromic 51 ADAMTS# 51 carcinoid cancer 51 JAK2 mutation 51 plasma kallikrein 51 neuro degenerative disorders 51 Childhood Disorder 51 Pathological gambling 51 immunodeficiency disease 51 polycystic ovary syndrome 51 Alzheimers disease 51 purpura ITP 51 Premature birth 51 systemic mastocytosis 51 Synovial Sarcoma 51 purpura 51 Alzheimer Disease AD 51 secondary hyperparathyroidism 51 missense mutation 51 MYH9 gene 51 primitive neuroectodermal tumors 51 chronic inflammatory bowel 51 VCFS 51 rare neurological disorder 51 Rh positive 51 fat malabsorption 51 debilitating neurodegenerative disorder 51 Rh incompatibility 51 mental retardation epilepsy 51 celiac disease digestive 51 Bacterial vaginosis 51 idiopathic pulmonary fibrosis IPF 51 polycystic disease 51 sinus node 51 Cardiac arrhythmia 51 recessively inherited 51 hemolytic disease 51 gastroparesis 51 systemic lupus erythematosus SLE 51 primary biliary cirrhosis 51 LRRK2 mutations 51 thoracic aortic aneurysm 51 Tardive dyskinesia 51 lung fibrosis 51 Duchenne muscular dystrophy 51 haemochromatosis 51 neonatal respiratory distress 51 neuroblastoma 51 respiratory insufficiency 51 Penile cancer 51 interstitial nephritis 51 Enlarged prostate 51 Cushing Syndrome 51 spontaneous mutation 51 imperfecta 51 encephalitis swelling 51 Chronic pancreatitis 51 Interstitial cystitis 51 Multiple myeloma 51 MECP2 gene 51 bacteria Pseudomonas aeruginosa 51 Acidosis 51 autoimmune thyroid 51 Sudden Unexplained Death 51 arrythmias 51 Goldenhar syndrome 51 dystrophin protein 51 diabetic kidney 51 degenerative retinal disease 51 neurodegenerative 51 electrical conduction 51 Progeria 51 juvenile idiopathic arthritis JIA 51 Idiopathic Pulmonary Fibrosis IPF 51 T1DM 51 Bulimia nervosa 51 Amblyopia 51 autosomal dominant inheritance 51 Chronic kidney 51 Congenital 51 onset diabetes 51 Uncontrolled diabetes 51 diaphragmatic hernia 51 Chronic myeloid leukemia CML 51 wet macular degeneration 51 bacterium Streptococcus 51 Congenital heart 51 Crouzon syndrome 51 juvenile myoclonic epilepsy 51 Cardiac hypertrophy 51 Treacher Collins Syndrome 51 protein tau 51 glial derived neurotrophic 51 pituitary adenoma 51 celiac sprue 51 Acute lymphoblastic leukemia 51 Zinc deficiency 51 bacterium Mycobacterium tuberculosis 51 neurological diseases 51 Osteogenesis imperfecta 51 NOTCH1 51 cardiac arrythmia 51 idiopathic cardiomyopathy 51 severe obstructive pulmonary 51 malformations 51 glycogen storage 51 Oxidative stress 51 Mitral regurgitation 51 disorders 51 Apolipoprotein E 51 Follicular lymphoma 51 mitochondrial diseases 51 disease 51 histiocytosis 51 dysregulated 51 optica 51 primary immunodeficiency 51 hypereosinophilic syndrome 51 inflammatory bowel diseases 51 Genetic predisposition 51 Pervasive Developmental Disorder 51 chronic rheumatic 51 Pelizaeus Merzbacher Disease 51 incurable degenerative 51 Bronchiectasis 51 neurodevelopmental disorders 51 Hypertrophic Cardiomyopathy HCM 51 Familial hypercholesterolemia 51 lactic acidosis 51 McCune Albright 51 pulmonary hypertension PH 51 Pleural mesothelioma 50 mucopolysaccharidosis 50 cerebral thrombosis 50 Wet AMD 50 Celiac sprue 50 motor neuropathy 50 chromosome #q#.# [001] 50 Primary IGFD 50 Neuropathic pain 50 common disabling neurological 50 Bronchiolitis 50 multiforme 50 chronic myeloid 50 ataxia 50 neurofibromatosis type 50 Crohns disease 50 idiopathic pulmonary 50 artery stenosis 50 adrenal hormones 50 lymphoblastic lymphoma 50 Anal cancer 50 enteropathy 50 Leber Congenital Amaurosis 50 HbF 50 fibrodysplasia ossificans progressiva FOP 50 bladder exstrophy 50 Myelofibrosis 50 nephrosis 50 Sjogren Syndrome 50 LRP5 50 Folate deficiency 50 Porphyria 50 mitochondrial mutations 50 Diabetic nephropathy 50 cerebral vasospasm 50 Cystic Fibrosis CF 50 pancreatitis inflammation 50 aplastic anemia rare 50 lymphoblastic leukemia 50 cirrhosis liver failure 50 Lennox Gastaut syndrome 50 hyperemesis 50 mycobacterium tuberculosis 50 clinically heterogeneous 50 interferon pathway 50 abnormal genital 50 interrupted aortic arch 50 dermatomyositis 50 alpha1 antitrypsin deficiency 50 chromosomal rearrangement 50 parasiticus 50 recessive gene 50 hypoplasia 50 Acute Myelogenous Leukemia AML 50 Wiskott Aldrich syndrome 50 tau pathology 50 Tuberous Sclerosis Complex 50 Infantile spasms 50 ankylosing spondylitis 50 Philadelphia Chromosome Positive 50 mutant gene 50 toxoplasmosis 50 crohn disease 50 diabetes insipidus 50 Spasmodic dysphonia 50 myoclonic epilepsy 50 onset Alzheimer disease 50 anaplastic lymphoma kinase 50 kidney disease 50 retinal dystrophies