dyskeratosis congenita

Related by string. * : / : arthrogryposis multiplex congenita . congenita * *

Related by context. Frequent words. (Click for all words.) 69 myotonic dystrophy 69 demyelinating disease 68 muscular dystrophies 68 familial ALS 68 Leber congenital amaurosis 68 TTR amyloidosis 67 autosomal recessive 67 neurodegenerative disorder 67 Atopic dermatitis 66 Myelofibrosis 66 Pulmonary hypertension 66 fatal neurodegenerative 66 anemias 66 HGPS 66 autosomal dominant 66 brain lesions 66 Angelman syndrome 66 RPE# 65 Duchenne muscular dystrophy DMD 65 optic neuropathy 65 colorectal carcinoma 65 muscle degeneration 65 degenerative disorder 65 hemolytic anemia 65 NF1 65 epidermolysis bullosa 65 Ischemic 64 lysosomal storage diseases 64 Metastases 64 Wegener granulomatosis 64 familial hypercholesterolemia 64 Amyotrophic lateral sclerosis 64 blood clotting disorder 64 coagulopathy 64 severe aplastic anemia 64 pancreatic adenocarcinoma 64 mitochondrial disorders 64 experimental autoimmune encephalomyelitis 64 mitochondrial dysfunction 64 Osteosarcoma 64 Cytomegalovirus 64 acute myelogenous leukemia AML 64 sporadic ALS 64 Obsessive compulsive disorder 64 degenerative neurological disorder 64 lung fibrosis 64 Coeliac disease 64 congenital disorders 64 paroxysmal nocturnal hemoglobinuria 64 NF2 64 rheumatoid arthritis lupus 64 Thrombocytopenia 64 Chronic fatigue 64 immunodeficiency 64 myelodysplasia 63 CMV infection 63 T#I [002] 63 dystrophy 63 eosinophilic esophagitis 63 Cushing syndrome 63 Joubert syndrome 63 Fanconi anemia 63 glomerulonephritis 63 progressive degenerative 63 carcinoid 63 nonsense mutation 63 ependymoma 63 Alzheimer Disease AD 63 cardiac hypertrophy 63 Lennox Gastaut syndrome 63 thrombophilia 63 Mucositis 63 Pancreatic 63 AAT deficiency 63 Hyperthyroidism 63 Retinopathy 63 progressive degeneration 63 hyperparathyroidism 63 Idiopathic 63 Hemorrhagic 63 hematopoietic cell 63 bronchopulmonary dysplasia 63 Muscular dystrophy 63 receiving VELCADE 62 pituitary tumors 62 neurological dysfunction 62 GRNCM1 62 purpura 62 Glioma 62 primary pulmonary hypertension 62 progressive neurodegenerative disease 62 DiGeorge syndrome 62 Retinoblastoma 62 nephritis 62 neurological disorder characterized 62 acute promyelocytic leukemia 62 thyroid dysfunction 62 pheochromocytoma 62 Genetic variation 62 Friedreich ataxia 62 uremia

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