Ellis Van Creveld Syndrome |
Exostoses, Multiple Hereditary |
Epidermolytic Hyperkeratoses |
Epilepsies, Juvenile Myoclonic |
Episodic Ataxia, Type 1 |
Episodic ataxia type 2 |
Enhanced S-Cone Syndrome |
Epidermolysis bullosa with pyloric atresia |
Encephalopathy, ethylmalonic |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy |
Epiphyseal dysplasia, multiple, 5 |
Epilepsies |
Epidermolysis Bullosa Dystrophica |
Epidermolysis Bullosa Simplex |
Erythrokeratodermia Variabilis |
Epidermolysis Bullosa, Junctional, Non-Herlitz Type |
Epidermolysis bullosa simplex, Ogna type |
Erythrocytosis, Familial, 2 |
Epilepsy, Nocturnal Frontal Lobe, Type 3 |
Eunuchoidism, familial hypogonadotropic |
Endocrine-Cerebroosteodysplasia |
Elliptocytoses, Hereditary |
Epidermodysplasia Verruciformis |
Esophageal Neoplasm |
Essential Thrombocythemias |
Epidermolysis Bullosa, Junctional |
Ectodermal Dysplasia 1, Anhidrotic |
Erythropoietic Protoporphyria |
Ectrodactyly-cleft lip-palate syndrome |
Epidermolysis Bullosa Pruriginosa |
Epilepsy, Lateral Temporal Lobe, Autosomal Dominant |
Ectodermal dysplasia, hypohidrotic, with immune deficiency |
Early-onset ataxia with oculomotor apraxia and hypoalbuminemia |
Enchondromatoses |
Epidermolysis bullosa simplex with mottled pigmentation |
Epidermolysis bullosa dystrophica, Pasini type |
Ectodermal Dysplasia-Skin Fragility Syndrome |
Ehlers-Danlos syndrome type 6 |
Epilepsy, Partial, with Variable Foci |
Epilepsy, Progressive, With Mental Retardation |
Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive |
Erythrokeratodermia Variabilis 3 |
Epithelial Recurrent Erosion Dystrophy |
Encephalocraniocutaneous lipomatosis |
Epiphyseal dysplasia, multiple, 1 |
Epiphyseal dysplasia, multiple, 4 |
Exudative vitreoretinopathy 1 |
Ectodermal dysplasia, ectrodactyly, and macular dystrophy |
Endplate Acetylcholinesterase Deficiency |
Epidermolysis bullosa, lethal acantholytic |
Ehlers-Danlos syndrome type 1 |
Epilepsy, Generalized, with Paroxysmal Dyskinesia |
Erythrokeratodermia with ataxia |
Ehlers-Danlos Syndrome, musculocontractural type 1 |
Epidermolysis Bullosa Simplex With Pyloric Atresia |
Ectopia Lentis, Spontaneous Filtering Blebs, and Craniofacial Dysmorphism |
Epilepsy, Female-Restricted, with Mental Retardation |
Encephaloclastic Proliferative Vasculopathy |
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations |
Episodic Ataxia, Type 6 |
Eiken Skeletal Dysplasia |
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip-Palate Syndrome 3 |
Epilepsy, Progressive Myoclonic 3 |
Epileptic Encephalopathy, Early Infantile, 4 |
Ectopia Lentis |
Eczema |
Epileptic Encephalopathy, Early Infantile, 3 |
Encephalitides, Herpes Simplex |
Esophageal Squamous Cell Carcinoma |
Epiphyseal dysplasia, multiple, 3 |
Epilepsy, Nocturnal Frontal Lobe, Type 4 |
Epilepsy, Nocturnal Frontal Lobe, Type 1 |
Epileptic Encephalopathy, Early Infantile, 2 |
Exudative Vitreoretinopathy, Familial, X-Linked Recessive |
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders |
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema |
Exostoses, Multiple, Type II |
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness |
Elliptocytosis 2 |
Erythrocytosis, Familial, 3 |
Erythrocyte Lactate Transporter Defect |
Ectodermal Dysplasia, Pure Hair-Nail Type |
Episodic Ataxia, Type 5 |
Exudative Vitreoretinopathy 4 |
Erythrocytosis, Familial, 4 |
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant |
Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive |
Exudative Vitreoretinopathy 5 |
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency |
Epileptic Encephalopathy, Early Infantile, 1 |
Epidermal Naevus |
Essential Hypertension |
Enterokinase Deficiency |
Ectopia Lentis with Ectopia of Pupil |
Epidermolysis Bullosa Simplex with Migratory Circinate Erythema |
Euthyroid Goiter |
Ehlers-Danlos syndrome caused by tenascin-X deficiency |
Ehlers Danlos Syndrome |
Endometrial Neoplasm |
Endometrioses |
Eosinophilia |
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails |
Enterocolitis, Necrotizing |
Ehlers-Danlos syndrome, cardiac valvular form |
Elliptocytosis 3 |
Epidermolysis Bullosa Dystrophica, Autosomal Recessive, Localisata Variant |
Epidermolysis Bullosa Dystrophica Inversa, Autosomal Recessive |
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis |
Elliptocytosis 1 |
Emery-Dreifuss Muscular Dystrophy 4 |
Erythrocyte Amp Deaminase Deficiency |
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive |
Enteropathies, Protein-Losing |
Endotoxemia |
Ectrodactyly |
Ehlers-Danlos syndrome type 2 |
Epilepsies, Rolandic |
Epilepsies, Temporal Lobe |
Esophageal Achalasia |
Encephalopathies, Hepatic |
Epidermolysis bullosa inversa dystrophica |
Edema |
Encephalomyelitis, Autoimmune Experimental |
Ependymoma |
Epilepsies, Generalized |
Erythromelalgia |
Experimental Liver Neoplasm |
Experimental Mammary Neoplasm |
Exfoliation Syndrome |
Ehlers-Danlos Syndrome, Type VIII |
Essential Tremor |
Esophagitides, Eosinophilic |
Epilepsies, Progressive Myoclonic |
Episodic Ataxia |
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 |
Epiphyseal dysplasia, multiple, 2 |
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like |
Estren-Dameshek Variant of Fanconi Anemia |
Estren-Dameshek Variant of Fanconi Pancytopenia |
Elejalde Disease |
Ehlers-Danlos syndrome, progeroid form |
Epidermolysis Bullosa, Junctional, Localisata Variant |
Ebsteins Anomaly |
Enterocolitides |
Ectodermal Dysplasias |
Emphysema |
Endometrial Hyperplasia |
Epilepsies, Myoclonic |
Epistaxis |
Exanthema |
Errors, Refractive |
Epilepsy, Frontal Lobe |
Exocrine Pancreatic Insufficiencies |
Edema, Macular |
Erdheim Chester Disease |
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp |
Ectopia lentis isolated |
Enlarged Vestibular Aqueduct |
Emery-Dreifuss Muscular Dystrophy 6, X-Linked |
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant |
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1 |
Epidermolysis Bullosa |
Esophagitides, Peptic |
Epilepsies, Partial |
Epilepsies, Drug Resistant |
Eaton Lambert Myasthenic Syndrome |
Error, Inborn Metabolism |
Erythema |
Epidermolysis Bullosa Simplex, Autosomal Recessive |
Encephalitis |
Esophagitides |
Experimental Neoplasm |
Eosinophilia Myalgia Syndrome |
Evans Syndrome |
End Stage Liver Disease |
Epilepsy, Myoclonic, Benign Adult Familial, Type 2 |
Extrahepatic Cholestasis |
Echinococcoses |
Emaciation |
Embolism |
Empty Sella Syndrome |
Endocrine Gland Neoplasm |
Entamoebiases |
Enteritides |
Enterovirus Infections |
Epilepsies, Tonic-Clonic |
Erythema Multiforme |
Escherichia coli Infection |
Esophageal and Gastric Varices |
Esophageal Stenoses |
Epithelial Neoplasm, Glandular |
Effusions, Pericardial |
Effusion, Pleural |
Ectopic Pregnancies |
Embolism and Thrombosis |
Epilepsy, Complex Partial |
Embolism, Cholesterol |
Eye Pains |
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified |
Encephalitis, Viral |
Ehlers-Danlos syndrome type 5 |
Endomyocardial Fibroses |
Epithelial ovarian cancer |
Embryo Loss |
Ectodermal Dysplasia 3, Anhidrotic |
Erythrokeratoderma, Reticular |
Epilepsy, Benign Neonatal, 3 |
Epidermolysis Bullosa Simplex Superficialis |
Exudative Vitreoretinopathy 3 |
Elliptocytosis 4 |
Ectopia Lentis, Isolated, Autosomal Recessive |
Epilepsy, Familial Adult Myoclonic, 3 |
Epiphyseal Dysplasia, Multiple, with Myopathy |
Encephalomyelitis |
Eclampsia |
Endophthalmitides |
Epididymitides |
Encephalopathies, Sepsis-Associated |
Esophageal atresia with or without tracheoesophageal fistula |
Endometritis |
Enterobacteriaceae Infection |
Euthyroid Sick Syndrome |
Eye Infection, Fungal |
Epilepsies, Reflex |
Egg Hypersensitivities |
Exostoses |
Epstein Barr Virus Infections |
Endemic Goiters |
Erythema Nodosum |
Exophthalmos |
Ehlers-Danlos syndrome type 3 |
Ectropion |
Encephalocele |
Exotropia |
Epilepsia Partialis Continua |
Enuresis, Nocturnal |
Endocardial Fibroelastoses |
Eye Neoplasm |
Epiretinal Membrane |
Earache |
Ecchymoses |
Echolalia |
Encephalitis, Japanese |
Encephalitis, St. Louis |
Encephalomalacia |
Endocarditides |
Endocarditis, Bacterial |
Endodermal Sinus Tumor |
Entropion |
Enuresis |
Epispadias |
Erysipelas |
Erythroblastoses, Fetal |
Esotropia |
Extraversion (Psychology) |
Epilepsy, Motor Partial |
Expiratory Volume, Forced |
Extramedullary Hematopoieses |
Edemas, Laryngeal |
Externa, Otitis |
Extramammary Pagets Disease |
Effusion, Malignant Pleural |
Euphoria |
Endometrial Stromal Tumor |
Ectopia pupillae |
Electrocardiography |
Epilepsy, Progressive Myoclonic 2B |
EDS VIIB |
Epilepsy, Childhood Absence, Susceptibility To, 4 |
Epilepsy, Benign Neonatal, 1, And-Or Myokymia |
Echogenic Bowel |
Epileptic Syndromes |
Encephalitides, Tick-Borne |
Endotoxin Hyporesponsiveness |
Elastosis perforans serpiginosa |
Esthesioneuroblastoma, Olfactory |
Elephantiases, Filarial |
Empyema |
Eccrine Porocarcinoma |
Ectromelia |
Encephalomyelitis, Venezuelan Equine |
Erythema Chronicum Migrans |
Endolymphatic Hydrops |
Emphysema, congenital lobar |
Eosinophilia, Familial |
Emotion, Expressed |
Emanuel syndrome |
Early-Onset Glaucoma |
Endocarditis, Subacute Bacterial |
Erythroplasia |
Eye Infections |
Emphysemas, Mediastinal |
Elbows, Tennis |
Epidermolysis Bullosa Acquisita |
Ehrlichioses |
Enthesopathy |
Eosinophilic gastroenteritis |
Episodic Kinesigenic Dyskinesia 2 |
Ear Neoplasm |
Echinococcoses, Hepatic |
Echinococcosis, Pulmonary |
Echovirus Infection |
Ecthyma |
Elephantiases |
Empyema, Pleural |
Enophthalmos |
Enterotoxemia |
Epidural Neoplasm |
Epiglottitides |
Epiphyses, Slipped |
Erysipelothrix Infections |
Esophageal Fistula |
Exanthema Subitum |
Exhibitionism |
Eye Manifestation |
Eyelid Neoplasm |
Effusion, Subdural |
Ectopic Junctional Tachycardias |
Erythema Infectiosum |
Encephalitozoonoses |
Enterobiases |
Eastern Equine Encephalomyelitides |
Embolism, Paradoxical |
Eosinophilic Fasciitis |
Eosinophilic gastritis |
Epidural Abscess |
Eales disease |
Enteropathies, HIV |
Eosinophilic pustular folliculitis |
Emergence Delirium |
Endemic Tyrolean Infantile Cirrhosis |
External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus |
Epilepsy, Familial Mesial Temporal Lobe |
Eating Syndromes, Night |
Episodic Ataxia, Type 7 |
External Ears |
Endothelium |
Eosinophil |
Epiphyses |
Erythrocyte |
Extremity |
Eye |
Eyelid |