Related by context. All words. (Click for frequent words.) 69 CHARGE syndrome 68 Joubert syndrome 64 brain malformation 64 chromosomal disorder 64 Crouzon Syndrome 63 Dravet syndrome 63 Angelman Syndrome 62 hemophagocytic lymphohistiocytosis 62 degenerative disorder 62 Krabbe Disease 62 DiGeorge syndrome 62 Mitochondrial Disease 62 Hypoplastic Left Heart 61 Usher Syndrome 61 Dravet Syndrome 61 epidermolysis bullosa EB 61 Aicardi Syndrome 61 holoprosencephaly 61 Diamond Blackfan Anemia 61 Aicardi syndrome 61 chromosome abnormality 61 Pompe Disease 61 mitochondrial disease 61 fibrodysplasia ossificans progressiva FOP 60 Pompe disease rare 60 Muscular dystrophy 60 quadriplegic cerebral palsy 60 Retinoblastoma 60 Prader Willi syndrome 60 Biliary Atresia 60 incurable neurological disorder 60 Von Willebrand disease 60 biliary atresia rare 60 Neurofibromatosis 60 Wiskott Aldrich Syndrome 60 Spina bifida 60 blastoma 60 Hutchinson Gilford Progeria 60 degenerative neurological disease 60 septo optic dysplasia 60 Diffuse Intrinsic Pontine Glioma 60 Krabbe Leukodystrophy 60 Niemann Pick disease 60 Angelman syndrome 60 Fanconi anemia 60 severe aplastic anemia 59 Fanconi anemia rare 59 Wilm tumor 59 leukodystrophy 59 neurofibromatosis 59 chromosomal defect 59 Down syndrome chromosomal disorder 59 Moebius Syndrome 59 Morquio syndrome 59 cystic fibrosis hereditary 59 juvenile myelomonocytic leukemia 59 Chiari malformation 59 Cerebral palsy 59 Alport Syndrome 59 Proteus Syndrome 59 Lafora disease 59 Rubinstein Taybi syndrome 59 spastic paraplegia 59 Hirschsprung disease 59 immunodeficiency disorder 59 incurable genetic 59 mitochondrial myopathy 59 Niemann Pick 59 degenerative muscular 58 Apert Syndrome 58 fronto temporal dementia 58 degenerative neurological disorder 58 congenital diaphragmatic hernia 58 Crigler Najjar syndrome 58 Anencephaly 58 Fragile X Syndrome 58 Rett Syndrome 58 Aplastic anemia 58 Sanfilippo syndrome 58 Tuberous Sclerosis 58 Battens Disease 58 Myocarditis 58 myotonic dystrophy 58 osteogenesis imperfecta 58 rare chromosomal disorder 58 optic nerve hypoplasia 58 ectodermal dysplasia 58 Von Hippel Lindau 58 genetic disorder 58 Polycystic Kidney Disease 58 Hydrocephalus 58 Krabbe disease 58 Hirschsprung Disease 58 DiGeorge Syndrome 58 CdLS 58 Hurler syndrome 58 spastic diplegia 58 Arnold Chiari Malformation 58 Ewing sarcoma bone 58 Treacher Collins syndrome 58 Morquio Syndrome 58 achondroplasia 58 Cardiomyopathy 57 lymphoblastic lymphoma 57 chiari malformation 57 Polycystic kidney disease 57 nonalcoholic cirrhosis 57 Wilms Tumor 57 Marfan Syndrome 57 Noonan Syndrome 57 uterus didelphys 57 Lewy Body Dementia 57 cerebellar ataxia 57 FRAXA Research 57 Angelman 57 Sanfilippo Syndrome 57 Apert syndrome 57 arthrogryposis 57 Hemochromatosis 57 recessive genetic 57 Medulloblastoma 57 Kawasaki Disease 57 neurofibromatosis NF 57 VCFS 57 lymphoblastic leukemia 57 spinal muscular atrophy 57 aplastic anemia rare 57 Duchene muscular dystrophy 57 degenerative neuromuscular disease 57 Spinal muscular atrophy 57 biliary atresia 57 Kufs disease 57 arthrogryposis multiplex congenita 57 Hutchinson Gilford progeria 57 Fanconi Anaemia 57 Barth Syndrome 56 debilitating neurological disorder 56 inherited neurological disorder 56 Ewings Sarcoma 56 Burkitt Lymphoma 56 psychosocial dwarfism 56 static encephalopathy 56 McCune Albright 56 amniotic fluid embolism 56 Amyotrophic lateral sclerosis ALS 56 Proteus syndrome 56 Pulmonary hypertension 56 adrenoleukodystrophy ALD 56 Chiari Malformation 56 Spina Bifida 56 Sudden Arrhythmia Death 56 neurodevelopment disorder 56 fatal neuromuscular disorder 56 Diamond Blackfan anemia 56 neuro degenerative disorder 56 Alagille syndrome 56 DiGeorge syndrome rare 56 congenital hydrocephalus 56 degenerative neurological condition 56 Fanconi Anemia 56 Osteosarcoma 56 dominantly inherited 56 transfusion syndrome 56 juvenile dermatomyositis 56 progressive neurodegenerative disorder 56 genetic syndromes 56 spinocerebellar ataxia 56 Pre eclampsia 56 hereditary degenerative 56 Spinal Muscular Atrophy 55 Hurler Syndrome 55 Sandhoff disease 55 dyskeratosis congenita 55 Dwarfism 55 Hypophosphatasia 55 Canavan Disease 55 Fetal Alcohol 55 Niemann Pick Disease 55 Osteogenesis imperfecta 55 embryonal rhabdomyosarcoma 55 neurofibromatosis genetic disorder 55 autism neurological disorder 55 Klippel Trenaunay Weber 55 chromosomal defects 55 progressive degenerative neurological 55 retinal dysfunction 55 Progeria 55 Wilm Tumor 55 CHARGE Syndrome 55 Twin Transfusion Syndrome 55 Hutchinson Gilford Progeria Syndrome 55 Arnold Chiari 55 Biliary atresia 55 anencephaly fatal 55 Treacher Collins 55 congenital glaucoma 55 muscular dystrophy cystic fibrosis 55 Li Fraumeni syndrome 55 neurological disorder affecting 55 Beckwith Wiedemann syndrome 55 blood clotting disorder 55 Chronic fatigue 55 hypertrophic cardiomyopathy HCM 55 Prader Willi Syndrome 55 Prader Willi 55 Goldenhar syndrome 55 Crouzon syndrome 55 Pelizaeus Merzbacher disease 55 Parkinsons Disease 55 moyamoya 55 Osteogenesis Imperfecta 55 spastic quadriplegic cerebral palsy 55 nonhereditary 55 von Hippel Lindau 55 Down syndrome 55 Spinal Muscular Atrophy SMA 54 truncus arteriosus 54 Lou Gherig disease 54 primary ciliary dyskinesia 54 cerebal palsy 54 Persistent Sexual Arousal 54 Cystic fibrosis CF 54 Parkinson degenerative 54 spastic cerebral palsy 54 Krabbe leukodystrophy 54 incurable neurological 54 Von Willebrand 54 spinal muscular atrophy SMA 54 debilitating neurological disease 54 Inflammatory Breast Cancer 54 mental retardation blindness 54 autosomal recessive genetic 54 cerebral palsey 54 autosomal dominant polycystic kidney 54 Sudden Unexplained Death 54 Treacher Collins Syndrome 54 cerebral palsy 54 Dystonia 54 Hodgkins Disease 54 skeletal dysplasia 54 anencephaly 54 neurobiological disorder 54 Cockayne syndrome 54 Langerhans Cell Histiocytosis 54 undiagnosed celiac disease 54 DIPG 54 Leukodystrophy 54 Rhabdomyosarcoma 54 Wolf Hirschhorn 54 Rh incompatibility 54 Mitochondrial disease 54 bronchopulmonary dysplasia 54 diaphragmatic hernia 54 born prematurely 54 cerebral palsy epilepsy 54 lysosomal diseases 54 muscular dystrophy 54 Trisomy 54 Pneumococcal meningitis 54 Leber hereditary optic neuropathy 54 osteogenesis imperfecta OI 54 Brugada Syndrome 54 dystonia neurological movement 54 disorder thalassemia 54 chromosomal abnormality 54 genetically inherited 54 Necrotizing Fasciitis 54 Maroteaux Lamy Syndrome 54 cerebellar hypoplasia 54 retinitis pigmentosa degenerative 54 myelogenous leukemia 54 incurable neurodegenerative disease 54 Amyotrophic lateral sclerosis 54 multisystem disease 54 inherited neurodegenerative 54 PIDD 54 Leber congenital amaurosis 54 Cerebral malaria 54 progressive neuromuscular 54 chronic granulomatous disease 53 complex neurobiological disorder 53 Ehlers Danlos 53 Lou Gherig Disease 53 alzheimer disease 53 Meckel Gruber 53 autoinflammatory diseases 53 chromosomal disorders 53 Genetic predisposition 53 Rett syndrome 53 Beckwith Wiedemann Syndrome 53 Shwachman Diamond Syndrome 53 Cholangiocarcinoma 53 Myelodysplastic syndrome 53 Lewy Body dementia 53 immunodeficiency disease 53 genetic lysosomal storage 53 congenital disorder 53 progressive neurodegenerative disease 53 primary immunodeficiency 53 craniopagus parasiticus 53 ARVD 53 congenital muscular dystrophy 53 Aspergers Syndrome 53 congenital birth defects 53 Ewings sarcoma 53 clotting disorder 53 HELLP 53 frontal temporal dementia 53 Marfan 53 twin transfusion 53 stem glioma 53 AAT Deficiency 53 medium chain acyl 53 Neuroblastoma 53 de novo mutations 53 progressive neurological disorder 53 polycystic kidneys 53 inherited mutations 53 chromosomal anomaly 53 encephalitis swelling 53 #q#.# deletion syndrome 53 angiosarcoma 53 congenital blindness 53 Motor neurone disease 53 hereditary spastic paraplegia 53 lysosomal storage diseases 53 spinal bifida 53 hereditary hemorrhagic telangiectasia 53 Leber Congenital Amaurosis LCA 53 neuroblastoma 53 Mermaid Syndrome 53 Severe Combined Immunodeficiency 53 Wilms tumor 53 Acute Myelogenous Leukemia 53 hepatoblastoma 53 Wegener Granulomatosis 53 histiocytosis 53 Coeliac disease 53 dwarfism 53 Brain Tumour 53 hereditary blindness 53 Autoimmune disorders 53 genetic neuromuscular disorder 53 Apert 53 polydactylism 53 spina bifida 53 Bleeding Disorder 53 Apraxia 53 placental abruption 53 Holoprosencephaly 53 Polycystic Ovarian Syndrome 53 alexia 53 autosomal recessive disease 53 Myopathy 53 choriocarcinoma 53 neuro developmental disorder 53 neuropsychiatric disorder 53 SIDS Sudden Infant Death 53 Sudden infant 53 mental retardation epilepsy 52 WAGR syndrome 52 Progeria Research 52 osteosarcoma bone 52 Usher syndrome 52 fatal neurodegenerative 52 congenital amputation 52 rhabdomyosarcoma 52 Wilms tumors 52 nephritis 52 beta thalassemia 52 Ehlers Danlos syndrome 52 Hemiplegia 52 congenital cataracts 52 neurodevelopmental disorder characterized 52 Autism Spectrum Disorder 52 Langerhans cell histiocytosis 52 neuromuscular disorder 52 degenerative motor neuron 52 epidermolysis bullosa 52 polycystic kidney disease 52 chromosomal imbalance 52 Amyloidosis 52 Long QT syndrome 52 progressive neurodegenerative 52 Fantabulous Kelly 52 congenital heart 52 microchimerism 52 mitochondrial disorders 52 syringomyelia 52 pulmonary atresia 52 inherited retinal degeneration 52 neuro muscular disorder 52 fatal neurodegenerative disorder 52 congenital abnormality 52 Eisenmenger syndrome 52 outgrow peanut allergy 52 Batten Disease 52 Patau syndrome 52 HGPS 52 Rhabdomyosarcoma rare 52 idiopathic cardiomyopathy 52 dilated cardiomyopathy 52 spina bifada 52 autistic tendencies 52 Lou Gehrigs disease 52 Pleural mesothelioma 52 leukemia 52 AML Leukemia 52 Dravet 52 Polycystic Ovary Syndrome 52 cystic fibrosis chronic pancreatitis 52 ependymoma 52 Acute Myeloid Leukaemia 52 myelodysplasia 52 cystic fibrosis 52 Sudden Adult 52 Genetic Variations 52 Fanconi anemia FA 52 epigenetic changes 52 Reye Syndrome 52 Adrenoleukodystrophy 52 neurodegenerative disorder 52 Lesch Nyhan syndrome 52 primordial dwarfism 52 Juvenile Arthritis 52 Long QT Syndrome 52 Joshua Frase 52 retinoblastoma 52 genetic abnormality 52 Retinitis pigmentosa 52 Childhood Disorder 52 interstitial pulmonary fibrosis 52 alveolar rhabdomyosarcoma 52 juvenile diabetes 52 Endometriosis 52 Neural tube defects 52 persistent pulmonary hypertension 52 Pervasive Developmental Disorders 52 hydrocephaly 52 Arthrogryposis 52 prosopagnosia 52 Hydrocephalus Association 52 Epidermolysis Bullosa EB 52 neuromuscular disease 52 Ectopia Cordis 52 Iron deficiency anemia 52 Friedrich Ataxia 52 Shy Drager syndrome 52 Becker muscular dystrophy 52 imperfecta 52 Huntington Chorea 52 spinal meningitis 52 toxemia 52 Motor Neurone 52 Epstein Barr Virus 52 medulloblastoma tumors 52 Alopecia Areata 52 anoxic brain injury 52 velo cardio facial 52 spina bifida defect 52 neurological disorder 52 rhabdoid 52 spina bifida cerebral palsy 52 Ataxia 52 spine incompletely closed 52 Myasthenia gravis 52 chiari 52 myelomeningocele 52 hemochromatosis 52 Cystic Fibrosis CF 52 intracranial haemorrhage 52 cerebri 52 Scleroderma Research 52 Lewy Body 52 Preeclampsia 51 juvenile rheumatoid arthritis 51 disorder FASD 51 systemic scleroderma 51 familial adenomatous polyposis 51 Perthes disease 51 Alport syndrome 51 genetic defect 51 hydrops 51 Fibrous Dysplasia 51 leukodystrophies 51 deafness neurological 51 metachromatic leukodystrophy 51 Downs Syndrome 51 Familial Dysautonomia 51 multisystem disorder 51 Tay Sachs disease 51 Dyspraxia 51 retinitis pigmentosa hereditary 51 petit mal seizures 51 Smith Lemli Opitz 51 atypical rhabdoid tumor 51 CHDs 51 Tay Sachs Disease 51 Cystic Fibrosis 51 optic atrophy 51 eosinophilic esophagitis 51 monogenic 51 chronic autoimmune disorder 51 subarachnoid haemorrhage 51 Fetal Alcohol Syndrome 51 Emphysema 51 primitive neuroectodermal tumors 51 cystic fibrosis sufferers 51 Eloysa Vasquez 51 Acute Lymphocytic Leukemia 51 Rathke cleft cyst 51 multiorgan 51 autism 51 Hereditary angioedema HAE 51 Leber congenital amaurosis LCA 51 microencephaly 51 ichthyosis 51 congential 51 Rett syndrome neurological disorder 51 Neimann Pick 51 Pervasive Developmental Disorder 51 Kleine Levin 51 Depression NARSAD 51 cystic kidney 51 Sudden Arrhythmic Death 51 Polycystic ovary syndrome PCOS 51 Porphyria 51 Farrah Fawcett dies 51 Henoch purpura 51 recessively inherited 51 asperger syndrome 51 bulbar polio 51 Moebius syndrome 51 Froguel 51 Anorexia nervosa 51 peripartum cardiomyopathy 51 IL#R 51 Erb palsy 51 ruptured brain aneurysm 51 mitochondrial dysfunction 51 metabolic disorder 51 Dysplasia 51 Nephrogenic Systemic Fibrosis NSF 51 hereditary deafness 51 Fetal alcohol 51 cerebral palsy blindness 51 Glioblastoma 51 Inflammatory Bowel 51 idiopathic pulmonary 51 Arrhythmogenic Right Ventricular Cardiomyopathy 51 dysgenesis 51 nephrosis 51 rare neurological disorder 51 primary pulmonary hypertension 51 Acute Leukemia 51 Astrocytoma 51 osteogenic sarcoma 51 Primary Immune Deficiency 51 inoperable brain tumor 51 medulla blastoma 51 spastic quadriplegia 51 Gastroparesis 51 dermatomyositis 51 Infant botulism 51 cerebral palsy neurological disorder 51 tricuspid atresia 51 mental retardation cerebral palsy 51 Combined Immune Deficiency 51 tuberous sclerosis complex 51 Cystinosis 51 Hemolytic Uremic Syndrome HUS 51 savior sibling 51 Hashimoto thyroiditis 51 Alzeheimer 51 Parkinson disease neurological disorder 51 Scleroderma 51 Chordoma 51 Reflex Sympathetic Dystrophy Syndrome 51 dysautonomia 51 brittle bone 51 renal failure interstitial lung 51 leptin deficiency 51 serotonin imbalance 51 Eosinophilic 51 Histiocytosis 51 lymphatic cystic hygroma 51 MECP2 gene 51 diffuse intrinsic pontine glioma 51 neurodevelopmental disorder 51 Aphasia 51 rhabdomyosarcoma rare 51 Ewing sarcoma rare 51 hereditary predisposition 51 polycystic ovary syndrome 51 Klinefelter syndrome 51 Toxoplasmosis 50 Brittle Bone Disease 50 neonatal encephalopathy 50 cortical dysplasia 50 Congenital Adrenal Hyperplasia 50 Ets2 50 neuroblastoma tumor 50 Attention Deficit Hyperactive Disorder 50 Churg Strauss syndrome 50 Celiac sprue 50 microvascular angina 50 Rotavirus infection 50 Genetic Variation 50 Glioma 50 mitochondrial defects 50 manic depressive disorder 50 pulmonary haemorrhage 50 Tye Blanton 50 roseola 50 Goldenhar Syndrome 50 ataxia telangiectasia 50 Aplastic Anemia 50 Ischaemic heart 50 facial deformity 50 lymphangioleiomyomatosis LAM 50 malformation 50 HELLP syndrome 50 multiforme 50 neurobehavioral disorder 50 Peritoneal mesothelioma 50 Crohns Disease 50 Friedreich ataxia 50 Wilms Tumour 50 microcephaly 50 non hodgkins lymphoma 50 osteopetrosis 50 debilitating neurodegenerative disorder 50 Obsessive compulsive disorder 50 blindness deafness 50 1 diabetes T1D 50 Hyperthyroidism 50 XMRV infection 50 Mitochondrial diseases 50 Klinefelter Syndrome 50 pseudotumor cerebri 50 tuberous sclerosis 50 protein dystrophin 50 primary sclerosing cholangitis 50 sporadic Creutzfeldt Jakob 50 genetic abnormalities 50 Lennox Gastaut syndrome 50 MCADD 50 fungal meningitis 50 Neonatal Death 50 subdural bleeding 50 neurogenetic disorders 50 unprovoked seizures 50 TTTS 50 MCAD deficiency 50 Dearly loved 50 IRF6 gene 50 Parasitic twins 50 measles encephalitis 50 Diabetic Ketoacidosis 50 systemic mastocytosis 50 Variant CJD 50 Pulmonary arterial hypertension 50 enzyme deficiency 50 Ectodermal Dysplasia 50 Juvenile Rheumatoid Arthritis 50 Cognitive Deficits 50 limb malformations 50 herpes encephalitis 50 hemolytic anemia 50 deafblindness 50 neonatal respiratory distress 50 neurogenetic 50 Selenium deficiency 50 oligodendrogliomas 50 Lou Gerhig disease 50 CDH1 50 meningococcal septicemia 50 mitochondrial mutations 50 viral myocarditis 50 hyperemesis gravidarum 50 heart valve stenosis 50 degenerative neurological 50 aplastic anemia 50 restrictive cardiomyopathy 50 neural tube birth defects 50 malignant glioma brain tumor 50 fatal neuromuscular 50 hypotonia 50 retinoblastoma rare 50 cystic fibrosis sickle cell 50 congenital kidney 50 Reflex Sympathetic Dystrophy RSD 50 NF2 50 recessive trait 50 neurodevelopmental disability 50 Asberger syndrome 50 dyscalculia 50 profound deafness 50 muscle degeneration 50 Pneumococcal pneumonia 50 spasmodic dysphonia 50 childhood disintegrative disorder 50 Acute Lymphoblastic Leukemia 50 Alzheimers disease 50 congenital hyperinsulinism 50 achromatopsia 50 Hodgkins Lymphoma 50 epilepsy neurological disorder 50 Polychronakos 50 Septicaemia 50 Rare Genetic 50 phthalate syndrome 50 Sickle Cell Anemia 50 hematological abnormalities 50 progeria rare 50 progressive retinal degenerative 50 cardiac channelopathies 50 Autism 50 degenerative retinal disease 50 Myositis 50 neurological impairments 50 spina bifida birth 50 Urologic Disease 50 pneumococcal meningitis 50 Peanut allergies 50 alpha thalassemia 50 Nonalcoholic fatty liver 50 autosomal dominant disorder 50 neuro degenerative disease 50 Gene Mutation Linked 50 Parkinsons disease 50 Postnatal depression 50 Tay Sachs 50 JMML 50 lissencephaly 50 National Alopecia Areata 50 motor neurone 50 compulsive hoarding 50 opsoclonus myoclonus syndrome 50 Raynaud disease 50 Chiplock 50 sacral agenesis 50 neuro muscular disease 50 Congenital heart 50 kernicterus 50 transplanted bone marrow 50 Burkitt lymphoma 50 Nephrotic Syndrome 50 dissociative amnesia 50 Tuberous Sclerosis Complex 50 neural tube defect 50 scleroderma chronic 50 Duchene Muscular Dystrophy 50 Parkinson Disease 50 Epidermolysis bullosa 50 IUGR 50 combined immunodeficiency SCID 50 paraneoplastic 50 mitochondrial diseases 50 neurodegenerative disorder characterized 50 variable immunodeficiency 50 FSGS 49 Cooley Anemia 49 myositis 49 biochemical imbalance 49 premature birth 49 Aortic dissection 49 recessive dystrophic epidermolysis bullosa 49 chromosome #q#.# deletion 49 Asperger Syndrome mild 49 Asperger Syndrome AS 49 hyperinsulinism 49 incurable degenerative brain 49 Peanut allergy 49 autism spectrum disorders 49 PANDAS 49 Hypertrophic Cardiomyopathy 49 underdeveloped lungs 49 neurodevelopmental disorders 49 Brain Aneurysm Foundation 49 cardio myopathy 49 SHANK3 gene 49 Asperger Disorder 49 cystic fibrosis muscular dystrophy 49 Cryptococcus neoformans 49 Asperger syndrome milder 49 AAT deficiency 49 Hodgkin Disease 49 diabetic kidney 49 Haemophilia 49 viral cardiomyopathy 49 craniosynostosis 49 Hypothyroidism 49 neuro degenerative 49 Acute Lymphoblastic Leukaemia 49 ErinoakKids 49 chromosome deletion 49 retinal blastoma 49 progressive neurodegenerative disorders 49 Newborn screening 49 Tuberous sclerosis 49 Prostrate cancer 49 immunodeficiency diseases 49 hereditary nonpolyposis colon cancer 49 verbal apraxia 49 Postpartum Depression 49 Carcinoid 49 bilateral retinoblastoma 49 proximal femoral focal 49 Retinopathy 49 Cardiac arrhythmia 49 ADA SCID 49 Kenadie 49 inherited genetic mutation 49 Knights Templar Eye 49 Leber Congenital Amaurosis 49 LRRK2 gene 49 herpes simplex encephalitis 49 defects mental retardation 49 paraganglioma 49 Austism 49 Charcot Marie Tooth 49 ruptured cerebral aneurysm 49 cerebral vascular disease 49 Lafora 49 vascular malformation 49 paralysis blindness 49 gene MECP2 49 Hemolytic Uremic Syndrome 49 CHD7 49 Beta thalassemia 49 Sclerosing 49 galactosemia 49 Dysautonomia 49 autosomal recessive 49 Multiple Births 49 Laurie Recht struggled 49 celebral palsy 49 hereditary disorder 49 ataxias 49 pre eclampsia 49 fibrous dysplasia 49 chronic obstructive airway 49 Kate Sofia Vassilieva 49 Down syndrome autism 49 gene p# 49 immunodeficiencies 49 muscular dystrophy cerebral palsy 49 Hemorrhagic stroke 49 Parkinson disease degenerative neurological 49 Premature birth 49 corticobasal degeneration rare 49 Coeliac Disease 49 LQTS 49 thyroid hormone deficiency 49 FASD 49 pyloric stenosis 49 Chronic Fatigue 49 debilitating arthritis 49 polymyositis 49 Sickle cell 49 Penile cancer 49 Acute lymphocytic leukemia 49 hormonal disorder 49 Graft Versus Host 49 interferon pathway 49 Myalgic Encephalomyelitis 49 Colorectal cancers 49 Alzhiemer 49 TTR amyloidosis 49 Transverse Myelitis 49 G#S mutation 49 Candida overgrowth 49 multi infarct dementia 49 Essential tremor 49 polycystic ovaries 49 severe congenital neutropenia 49 incurable degenerative 49 polymorphic ventricular tachycardia 49 degenerative nerve 49 GPC5 49 Premature Ovarian Failure 49 bicuspid valve 49 encephalitis meningitis 49 aneuploidies 49 NPHP 49 infertility miscarriages 49 P. aeruginosa infection 49 Pulmonary fibrosis 49 brain haemorrhages 49 grandmother Betty Hockin 49 grand mal seizures 49 Retinitis Pigmentosa RP 49 pulmonary thromboembolism 49 ruptured uterus 49 CFS ME 49 Motor Neuron 49 cardiomyopathy weakening 49 neurological degeneration 49 Chronic pancreatitis 49 hippocampal function 49 polycystic ovarian syndrome PCOS 49 Lennox Gastaut Syndrome 49 Budd Chiari syndrome 49 synovial sarcoma 49 hereditary nonpolyposis colorectal cancer 49 Bardet Biedl Syndrome 49 bacterium Streptococcus pneumoniae 49 neuroblastomas 49 congenital scoliosis 49 haemochromatosis 49 Interstitial cystitis 49 Syringomyelia 49 lactase deficiency 49 autism Asperger 49 Congenital Diaphragmatic Hernia 49 immuno deficiency 49 reflex sympathetic dystrophy 49 apraxia 49 savant syndrome 49 congenital abnormalities 49 inherited neurodegenerative disorder 49 Hazelle Roa 49 Myasthenia Gravis 49 cryptogenic cirrhosis 49 Cerebral palsy involves 49 congenital deafness 49 SHANK3 49 Neurofibromatosis Type 49 myotonic muscular dystrophy 49 pulmonary fibrosis lung 49 myopathies 49 Cystic fibrosis 49 primary biliary cirrhosis 49 neurological disorders orphan 49 Ohtahara syndrome rare 49 sickle hemoglobin 49 Marfan syndrome 49 septicemic 49 epilepsy 49 neurofibroma 49 filaggrin 49 Zinc deficiency 49 arteriovenous malformation AVM 49 nasal pharyngeal cancer 49 Alzheimers Disease 49 chronic progressive neurodegenerative 49 Foetal alcohol 49 airway blockage 49 neurofibromatosis type 49 Erb Palsy 49 ceroid lipofuscinosis NCL 49 congenital disorders 49 myasthenia gravis neuromuscular 49 nasopharyngeal carcinoma NPC 49 Tourette Syndrome TS 49 Malyia 49 epidural hematoma bleeding 49 Lactose intolerance 49 Tourette syndrome neurological disorder 49 Gairett 49 spinal muscle atrophy 49 vWD 48 Persistent Pulmonary Hypertension 48 Sturge Weber syndrome 48 carcinoid cancer 48 hereditary disorders 48 Non Hodgkins lymphoma 48 premature babies 48 inherited degenerative 48 Atopic dermatitis 48 Premature Birth 48 FightSMA 48 interstitial nephritis 48 Adenoid Cystic Carcinoma 48 Polycystic ovary syndrome 48 ADPKD 48 Duchenne muscular dystrophy DMD 48 idiopathic epilepsy 48 Kifuji diagnosed 48 motor neuron disease 48 Gene Linked 48 MEF2A 48 Capgras syndrome 48 myalgic encephalomyelitis ME 48 Malignant mesothelioma 48 Dental fluorosis 48 RPE# 48 Ewing Sarcoma 48 Congestive heart failure 48 leiomyosarcoma rare 48 Idiopathic pulmonary fibrosis 48 Testicular Cancer 48 TACI mutations 48 Neurofibromatosis type 48 Glioblastoma Multiforme 48 lymphatic leukemia 48 congenital cataract 48 lateral sclerosis ALS