|
Breast Carcinoma
|
|
Craniofacial Abnormalities
|
|
Prostatic Neoplasms
|
|
Liver Cirrhosis, Experimental
|
|
Hepatocellular Carcinoma
|
|
Colonic Neoplasm
|
|
Lung Neoplasms
|
|
Urinary Bladder Neoplasms
|
|
Colorectal Cancer
|
|
Cell Transformation, Neoplastic
|
|
Carcinoma, Adenoid Cystic
|
|
Stomach Neoplasms
|
|
Autism
|
|
Adenocarcinoma
|
|
Diabetes Mellitus, Type 2
|
|
Endometriosis
|
|
Intellectual Disability
|
|
Pancreatic Carcinoma
|
|
Ovarian Neoplasms
|
|
Autism Spectrum Disorder
|
|
Carcinoma
|
|
Squamous Cell Carcinoma
|
|
Diabetes Mellitus, Experimental
|
|
Liver Neoplasms
|
|
Esophageal Squamous Cell Carcinoma
|
|
Melanoma
|
|
Neoplasm Invasiveness
|
|
Small Cell Lung Carcinoma
|
|
Lung Adenocarcinoma
|
|
Glioblastoma Multiforme
|
|
Mesothelioma, Malignant
|
|
Neoplasm Metastasis
|
|
Endometrial Neoplasm
|
|
Mammary Neoplasms, Experimental
|
|
Osteosarcoma
|
|
Leukemia, Myeloid, Acute
|
|
Disease Progression
|
|
Insulin Resistance
|
|
Medulloblastoma
|
|
Carcinoma, Transitional Cell
|
|
Brain Ischemia
|
|
Hypertension
|
|
Neoplasms
|
|
Adrenocortical Carcinoma
|
|
Nervous System Diseases
|
|
Arthritis, Juvenile
|
|
Leukemia
|
|
Glioma
|
|
Cholangiocarcinoma
|
|
Skin Neoplasms
|
|
Carcinoma, Non-Small-Cell Lung
|
|
Rheumatoid Arthritis
|
|
Renal Cell Carcinoma
|
|
Mammary Neoplasms, Animal
|
|
Polycystic Ovary Syndrome
|
|
Neoplasm Recurrence, Local
|
|
Leukemia, Myeloid
|
|
Uterine Cervical Neoplasms
|
|
Cardiac Hypertrophy
|
|
Neoplasms, Experimental
|
|
Reperfusion Injury
|
|
Astrocytoma
|
|
Arsenic Poisoning
|
|
Esophageal Neoplasms
|
|
Obesity
|
|
Sarcoma
|
|
Thyroid Carcinoma
|
|
Brain Injuries
|
|
Kidney Failure, Chronic
|
|
Seizures
|
|
Cocaine Dependence
|
|
Infertility, Female
|
|
Male Infertility
|
|
Acute Lymphoblastic Leukemia
|
|
Lymphoma, T-Cell, Cutaneous
|
|
Sezary Syndrome
|
|
Lymphoma, T-Cell
|
|
Prostatic Intraepithelial Neoplasia
|
|
Fatty Liver
|
|
Hand Deformities, Congenital
|
|
Osteoarthritis
|
|
Brain Neoplasms
|
|
Arthritis, Experimental
|
|
Myocardial Infarction
|
|
Epilepsy
|
|
Drug-Induced Liver Injury
|
|
Skin Diseases
|
|
Alzheimer's Disease
|
|
Neoplasms, Germ Cell And Embryonal
|
|
Deafness
|
|
Microcephaly
|
|
Mesothelioma
|
|
Heat Stroke
|
|
Myelodysplastic Syndromes
|
|
Anxiety Disorder
|
|
Hemangiosarcoma
|
|
Neural Tube Defects
|
|
Neuroblastoma
|
|
Congenital Abnormalities
|
|
Abnormalities, Multiple
|
|
Acute Kidney Injury
|
|
Leukemia, Megakaryoblastic, Of Down Syndrome
|
|
Hiv Infections
|
|
Tooth Abnormalities
|
|
Amphetamine-Related Disorders
|
|
Neuroendocrine Tumors
|
|
Leukemia, Promyelocytic, Acute
|
|
Leukemia, Myelomonocytic, Juvenile
|
|
Basal Cell Carcinoma
|
|
Chronic Lymphocytic Leukemia
|
|
Lymphoma, Large B-Cell, Diffuse
|
|
Schizophrenia
|
|
De Lange Syndrome
|
|
Uterine Neoplasms
|
|
Heart Defects, Congenital
|
|
Lymphoma
|
|
Amyotrophic Lateral Sclerosis 1
|
|
Hyperplasia
|
|
Adenocarcinoma Of Esophagus
|
|
Heart Diseases
|
|
Burkitt Lymphoma
|
|
Heart Failure
|
|
Coffin-Siris Syndrome
|
|
Thymoma
|
|
Carcinoma, Squamous Cell Of Head And Neck
|
|
Familial Primary Pulmonary Hypertension
|
|
Cardiomyopathies
|
|
Crohn's Disease
|
|
Peripheral Neuropathy
|
|
Head And Neck Neoplasms
|
|
Myocardial Ischemia
|
|
Atherosclerosis
|
|
Androgenetic Alopecia
|
|
Toxic Epidermal Necrolysis
|
|
Status Epilepticus
|
|
Inflammation
|
|
Adenoma
|
|
Alcoholic Liver Cirrhosis
|
|
Disease Models, Animal
|
|
Ischemia
|
|
Spinocerebellar Ataxias
|
|
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
|
|
Lipidoses
|
|
Limb Deformities, Congenital
|
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
|
Kidney Disease
|
|
Psoriasis
|
|
Ceroid Lipofuscinosis, Neuronal 1, Infantile
|
|
Nerve Degeneration
|
|
Pulmonary Fibrosis
|
|
Nerve Sheath Neoplasms
|
|
Mouth Diseases
|
|
Recurrence
|
|
Mouth Neoplasms
|
|
Growth Disorders
|
|
Leukemia, Monocytic, Acute
|
|
Glucose Intolerance
|
|
Microsatellite Instability
|
|
Multiple Myeloma
|
|
Muscular Atrophy
|
|
Asthma
|
|
Hearing Loss
|
|
Nasopharyngeal Carcinoma
|
|
Corneal Dystrophy, Posterior Polymorphous, 1
|
|
Nervous System Malformations
|
|
Neurilemmoma
|
|
Coronary Artery Disease
|
|
Hepatoblastoma
|
|
Aging, Premature
|
|
Non-Alcoholic Fatty Liver Disease
|
|
Hernia, Diaphragmatic
|
|
Hernias, Diaphragmatic, Congenital
|
|
Carcinoma, Pancreatic Ductal
|
|
Hyperglycemia
|
|
Carcinoma, Small Cell
|
|
Ovarian Epithelial Cancer
|
|
Pancreatic Agenesis, Congenital
|
|
Pancreatitis
|
|
Parkinsonian Disorders
|
|
Acute Lung Injury
|
|
Peters Anomaly
|
|
Adrenal Gland Neoplasms
|
|
Barrett's Esophagus
|
|
Pilomatrixoma
|
|
Pituitary Hormone Deficiency, Combined, 2
|
|
Beckwith-Wiedemann Syndrome
|
|
Polycystic Kidney, Autosomal Dominant
|
|
Cecal Neoplasms
|
|
Precancerous Conditions
|
|
Central Nervous System Neoplasms
|
|
Primary Ovarian Insufficiency
|
|
Drug-Related Side Effects And Adverse Reactions
|
|
Keratoconus
|
|
Keratosis
|
|
Psychomotor Disorders
|
|
Chronic Obstructive Pulmonary Disease
|
|
Dwarfism
|
|
Bone Diseases, Developmental
|
|
Bone Neoplasms
|
|
Bowen's Disease
|
|
Uterine Fibroid
|
|
Brachydactyly
|
|
Aortic Aneurysm
|
|
Rett Syndrome
|
|
Leukemia-Lymphoma, Adult T-Cell
|
|
Rhabdomyosarcoma, Alveolar
|
|
Ulcerative Colitis
|
|
Chloracne
|
|
Rubinstein-Taybi Syndrome
|
|
Ewing Sarcoma
|
|
Leukemia, T-Cell
|
|
Liver Cirrhosis
|
|
Primary Biliary Cirrhosis
|
|
Liver Diseases, Parasitic
|
|
Liver Neoplasms, Experimental
|
|
Substance Withdrawal Syndrome
|
|
Eye Abnormalities
|
|
Facies
|
|
Testicular Neoplasms
|
|
Fanconi Anemia
|
|
Thoracic Neoplasms
|
|
Female Urogenital Diseases
|
|
Chromosome Breakage
|
|
Lymphoma, Follicular
|
|
Turcot Syndrome
|
|
Fibrous Dysplasia Of Bone
|
|
Breast Neoplasms, Male
|
|
Uveal Melanoma
|
|
Ventricular Remodeling
|
|
Meier-Gorlin Syndrome
|
|
Meningioma
|
|
Gallbladder Neoplasm
|
|
Waardenburg Syndrome Type 2
|
|
Cognitive Impairment
|
|
Genetic Predisposition To Disease
|
|
Colitis
|
|
Nephroblastoma
|
|
Glomerulonephritis
|
|
Megalencephaly
|
|
Meningioma, Familial
|
|
Mental Retardation, Autosomal Dominant 1
|
|
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1
|
|
Mental Retardation, X-Linked
|
|
Mental Retardation, X-Linked 79
|
|
Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related
|
|
Mercury Poisoning, Nervous System
|
|
Metabolic Diseases
|
|
Metabolic Syndrome X
|
|
Micronuclei, Chromosome-Defective
|
|
Microphthalmia, Syndromic 3
|
|
Microphthalmos
|
|
Migraine Disorder
|
|
Mitochondrial Diseases
|
|
Mody, Type 6
|
|
Movement Disorder
|
|
Muir-Torre Syndrome
|
|
Mulibrey Nanism
|
|
Multiple Endocrine Neoplasia Type 1
|
|
Muscle Hypotonia
|
|
Muscular Diseases
|
|
Muscular Dystrophy, Animal
|
|
Musculoskeletal Abnormalities
|
|
Musculoskeletal Pain
|
|
Myelodysplastic-Myeloproliferative Diseases
|
|
Myeloperoxidase Deficiency
|
|
Myoclonus
|
|
Myotonic Dystrophy
|
|
Nasopharyngeal Neoplasm
|
|
Nemaline Myopathy 2
|
|
Neoplasms, Squamous Cell
|
|
Neovascularization, Pathologic
|
|
Neuroectodermal Tumors, Primitive
|
|
Neurofibroma
|
|
Neurotoxicity Syndromes
|
|
Nevi And Melanomas
|
|
Nevus, Epithelioid And Spindle Cell
|
|
Nevus, Pigmented
|
|
Nicolaides Baraitser Syndrome
|
|
No-Reflow Phenomenon
|
|
Occupational Diseases
|
|
Ocular Hypertension
|
|
Oculootoradial Syndrome
|
|
O'Donnell Pappas Syndrome
|
|
Oligodendroglioma
|
|
Oligospermia
|
|
Ophthalmoplegia, Chronic Progressive External
|
|
Opitz-Kaveggia Syndrome
|
|
Optic Nerve Diseases
|
|
Optic Nerve Hypoplasia, Bilateral
|
|
Oral Submucous Fibrosis
|
|
Ovarian Cysts
|
|
Pallister-Hall Syndrome
|
|
Papilloma
|
|
Papilloma, Choroid Plexus
|
|
Paraganglioma
|
|
Paraquat Lung
|
|
Partington X-Linked Mental Retardation Syndrome
|
|
Penile Diseases
|
|
Penile Neoplasms
|
|
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease
|
|
Peritoneal Neoplasms
|
|
Phyllodes Tumor
|
|
Piebaldism
|
|
Pierre Robin Syndrome
|
|
Pigmentation Disorders
|
|
Pitt-Hopkins Syndrome
|
|
Pituitary Acth Hypersecretion
|
|
Pituitary Hormone Deficiency, Combined, 1
|
|
Plaque, Atherosclerotic
|
|
Pneumonia
|
|
Polycystic Kidney, Autosomal Recessive
|
|
Polydactyly
|
|
Polydactyly, Postaxial
|
|
Polydactyly, Preaxial 4
|
|
Polyendocrinopathies, Autoimmune
|
|
Polyploidy
|
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
|
|
Premature Ovarian Failure 7
|
|
Prenatal Exposure Delayed Effects
|
|
Primary Myelofibrosis
|
|
Primary Ovarian Insufficiency, Fragile X-Associated
|
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 1
|
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive
|
|
Propping Zerres Syndrome
|
|
Prostatic Neoplasms, Castration-Resistant
|
|
Proud Syndrome
|
|
Psychoses, Substance-Induced
|
|
Psychosis
|
|
Leigh Necrotizing Encephalopathy Due To Pyruvate Carboxylase Deficiency
|
|
Radiation Injuries, Experimental
|
|
Rapp-Hodgkin Syndrome
|
|
Rectum Cancer
|
|
Reflex, Abnormal
|
|
Respiratory Insufficiency
|
|
Restless Legs Syndrome
|
|
Reticuloendotheliosis, Familial, With Eosinophilia
|
|
Retinal Degeneration
|
|
Retinal Diseases
|
|
Cone-Rod Dystrophy 2
|
|
Rhabdoid Tumor Predisposition Syndrome 2
|
|
Rhabdomyosarcoma, Embryonal
|
|
Riddle Syndrome
|
|
Ring Dermoid Of Cornea
|
|
Salivary Gland Neoplasm
|
|
Sarcoma Family Syndrome Of Li And Fraumeni
|
|
Systemic Scleroderma
|
|
Scoliosis
|
|
Sebaceous Gland Neoplasms
|
|
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis
|
|
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive
|
|
Shock, Hemorrhagic
|
|
Shprintzen Golberg Craniosynostosis
|
|
Siderius X-Linked Mental Retardation Syndrome
|
|
Sinonasal Undifferentiated Carcinoma
|
|
Skin Abnormalities
|
|
Sotos Syndrome
|
|
Spinal Dysraphism
|
|
Spinocerebellar Ataxia 17
|
|
Splenomegaly
|
|
Split-Hand-Foot Malformation 4
|
|
Spondylarthritis
|
|
Stereotypic Movement Disorder
|
|
Stomatognathic System Abnormalities
|
|
Striatonigral Degeneration Infantile
|
|
Stroke
|
|
Drug Dependence
|
|
Sweat Gland Neoplasms
|
|
Syndactyly, Type V
|
|
Synpolydactyly 1
|
|
Tetralogy Of Fallot
|
|
Thoracic Diseases
|
|
Thrombocytopenia
|
|
Thrombocytopenia, Platelet Dysfunction, Hemolysis, And Imbalanced Globin Synthesis
|
|
Thymus Neoplasms
|
|
Thyroid Cancer, Follicular
|
|
Thyroid Cancer, Papillary
|
|
Tietz Syndrome
|
|
T-Lymphocytopenia
|
|
Tongue Neoplasms
|
|
Townes-Brocks Syndrome
|
|
Transient Myeloproliferative Disorder Of Down Syndrome
|
|
Trichuriasis
|
|
Trigeminal Neuralgia
|
|
Upper Extremity Deformities, Congenital
|
|
Uremia
|
|
Urogenital Neoplasms
|
|
Urologic Neoplasms
|
|
Urticaria
|
|
Vater Association
|
|
Vertical Talus, Congenital
|
|
Vipoma
|
|
Vision Disorders
|
|
Vitamin A Deficiency
|
|
Vulvar Lichen Sclerosus
|
|
Waardenburg Syndrome
|
|
Waardenburg Syndrome Type 2a
|
|
Waardenburg Syndrome, Type 2d
|
|
Waardenburg Syndrome, Type 4c
|
|
Weaver Syndrome
|
|
Werner Syndrome
|
|
Williams Syndrome
|
|
Wittwer Syndrome
|
|
Wounds And Injuries
|
|
46, Xx Disorders Of Sex Development
|
|
Yemenite Deaf-Blind Hypopigmentation Syndrome
|
|
46, Xy Disorders Of Sex Development
|
|
46, Xy Sex Reversal 5
|
|
Aberrant Crypt Foci
|
|
Acrocallosal Syndrome
|
|
Acromicric Dysplasia
|
|
Adenocarcinoma, Clear Cell
|
|
Adenoma, Liver Cell
|
|
Adenomatous Polyposis Coli
|
|
Adjustment Disorders
|
|
Adrenal Insufficiency
|
|
Adrenocortical Carcinoma, Hereditary
|
|
Advanced Sleep-Phase Syndrome, Familial
|
|
Agenesis Of Corpus Callosum
|
|
Albinism Ocular Late Onset Sensorineural Deafness
|
|
Albinism, Oculocutaneous
|
|
Alcoholic Intoxication
|
|
Alcohol Dependence
|
|
Alpha-Thalassemia Myelodysplasia Syndrome
|
|
Amelogenesis Imperfecta, Type Iv
|
|
Amyotrophic Lateral Sclerosis
|
|
Androgen-Insensitivity Syndrome
|
|
Anemia
|
|
Aneurysm, Dissecting
|
|
Angelman Syndrome
|
|
Aniridia
|
|
Aniridia Cerebellar Ataxia Mental Deficiency
|
|
Aniridia, Type 2
|
|
Anonychia Congenita
|
|
Anophthalmos
|
|
Anovulation
|
|
Anoxia
|
|
Aortic Valve, Calcification Of
|
|
Arterial Occlusive Diseases
|
|
Psoriatic Arthritis
|
|
Arthrogryposis
|
|
Atrial Fibrillation
|
|
Atrial Septal Defect 2
|
|
Atr-X Syndrome
|
|
Auditory Perceptual Disorders
|
|
Autoimmune Polyendocrinopathy Syndrome, Type 1
|
|
Balkan Nephropathy
|
|
Basal Cell Nevus Syndrome
|
|
Bile Duct Neoplasms
|
|
Bipolar Disorder
|
|
Body Weight
|
|
Bone Diseases, Metabolic
|
|
Brachydactyly-Syndactyly Syndrome
|
|
Brachydactyly, Type D
|
|
Brain Diseases
|
|
Branchiootic Syndrome 3
|
|
Branchio-Oto-Renal Syndrome
|
|
Breast Diseases
|
|
Bulbospinal Neuronopathy, X-Linked Recessive
|
|
Burns
|
|
Cafe Au Lait Spots, Multiple
|
|
Calcinosis
|
|
Campomelic Dysplasia
|
|
Candidiasis
|
|
Carcinogenesis
|
|
Carcinoma, Ductal, Breast
|
|
Carcinoma, Mucoepidermoid
|
|
Dilated Cardiomyopathy
|
|
Cardiomyopathy, Hypertrophic
|
|
Cardiovascular Abnormalities
|
|
Cardiovascular Disease
|
|
Carotid Artery Diseases
|
|
Carotid Intimal Medial Thickness 1
|
|
Cartilage Diseases
|
|
Cataract
|
|
Cataract, Autosomal Dominant
|
|
Cerebellar Diseases
|
|
Cerebrooculofacioskeletal Syndrome 1
|
|
Cervical Intraepithelial Neoplasia
|
|
Charcot-Marie-Tooth Disease
|
|
Charcot-Marie-Tooth Disease, Type 1d
|
|
Charcot-Marie-Tooth Disease, Type 4e
|
|
Charge Syndrome
|
|
Char Syndrome
|
|
Child Development Disorders, Pervasive
|
|
Cholestasis
|
|
Chromosome 17 Deletion
|
|
Chromosome 2q37 Deletion Syndrome
|
|
Chromosome Aberrations
|
|
Chronobiology Disorders
|
|
Classical Lissencephalies And Subcortical Band Heterotopias
|
|
Cleft Lip
|
|
Cleft Palate
|
|
Cleidocranial Dysplasia
|
|
Cockayne Syndrome
|
|
Coloboma
|
|
Coloboma Of Optic Nerve
|
|
Combined Cellular And Humoral Immune Defects With Granulomas
|
|
Congenital Central Hypoventilation Syndrome
|
|
Copper-Overload Cirrhosis
|
|
Corneal Dystrophies, Hereditary
|
|
Corneal Dystrophy, Fuchs Endothelial, 6
|
|
Corneal Dystrophy, Posterior Polymorphous, 3
|
|
Coronary Artery Disease, Autosomal Dominant, 1
|
|
Craniofacial Deafness Hand Syndrome
|
|
Craniopharyngioma
|
|
Craniosynostoses
|
|
Critical Illness
|
|
Cryptorchidism
|
|
Cystitis
|
|
Deafness, Autosomal Dominant 23
|
|
Deafness, Autosomal Dominant 28
|
|
Dementia
|
|
Demyelinating Diseases
|
|
Unipolar Depression
|
|
Major Depression
|
|
Dermatitis
|
|
Dermatitis, Allergic Contact
|
|
Dermatitis, Contact
|
|
De Sanctis-Cacchione Syndrome
|
|
Developmental Disabilities
|
|
Gestational Diabetes
|
|
Diabetes Mellitus
|
|
Diabetes Mellitus, Permanent Neonatal, With Cerebellar Agenesis
|
|
Diabetic Angiopathies
|
|
Diabetic Nephropathy
|
|
Diffuse Cerebral Sclerosis Of Schilder
|
|
Down Syndrome
|
|
Drug Eruptions
|
|
Duane Retraction Syndrome
|
|
Ductus Arteriosus, Patent
|
|
Duodenal Ulcer
|
|
Dwarfism, Pituitary
|
|
Dyslipidemias
|
|
Early-Onset Ataxia With Oculomotor Apraxia And Hypoalbuminemia
|
|
Ectopia Pupillae
|
|
Ectrodactyly-Cleft Lip-Palate Syndrome
|
|
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 3
|
|
Embryo Loss
|
|
Emphysema
|
|
Empty Sella Syndrome
|
|
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations
|
|
Endometrial Hyperplasia
|
|
Epileptic Encephalopathy, Early Infantile, 1
|
|
Fanconi Anemia, Complementation Group J
|
|
Feminization
|
|
Fetal Death
|
|
Fetal Growth Retardation
|
|
Fibroadenoma
|
|
Foot Deformities, Congenital
|
|
Fragile X Syndrome
|
|
Fragile X Tremor Ataxia Syndrome
|
|
Gait Ataxia
|
|
Gastrinoma
|
|
Gastrointestinal Diseases
|
|
Genital Diseases, Male
|
|
Focal Segmental Glomerulosclerosis
|
|
Glucagonoma
|
|
Gonadal Dysgenesis
|
|
Gonadal Dysgenesis, 46,Xx
|
|
Gonadal Dysgenesis, 46,Xy
|
|
Greig Cephalopolysyndactyly Syndrome
|
|
Growth Mental Deficiency Syndrome Of Myhre
|
|
Hay-Wells Syndrome
|
|
Hearing Disorders
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Heart Septal Defects
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Heart Valve Diseases
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Hemorrhage
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Hepatitis
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Hepatitis B
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Hepatitis C
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Hepatitis, Chronic
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Hepatolenticular Degeneration
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Hepatomegaly
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Hereditary Breast And Ovarian Cancer Syndrome
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Hereditary Sensory And Autonomic Neuropathies
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Hereditary Sensory And Motor Neuropathy
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Cyclopia
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Holoprosencephaly 4
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Holoprosencephaly 9
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Hydrocephalus
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Hyperalgesia
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Hyperkinesis
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Hyperoxaluria
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Hyperparathyroidism 1
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Pulmonary Hypertension
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Hypogonadism
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Hypokalemia
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Hypopigmentation
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Hypopituitarism And Septooptic 'Dysplasia'
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Hypospadias 1, X-Linked
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Hypothalamic Hamartomas
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Hypothyroidism, Congenital, Nongoitrous, 5
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Hypotrichosis Simplex
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Idiopathic Hypogonadotropic Hypogonadism
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Immunoblastic Lymphadenopathy
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Immunologic Deficiency Syndromes
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Infarction, Middle Cerebral Artery
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Insulinoma
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Intestinal Neoplasms
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Intestinal Polyps
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Iridogoniodysgenesis, Dominant Type
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Jaw Abnormalities
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Juvenile Polyposis Syndrome
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Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia
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Kallmann Syndrome
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Keloid
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Keratitis, Hereditary
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Keratoconus 1
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Kidney Neoplasms
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Kidney Tubular Necrosis, Acute
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Kyphosis
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Laron Syndrome Type 2
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Learning Disorders
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Leber Congenital Amaurosis
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Leiomyosarcoma
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Leukemia, Large Granular Lymphocytic
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Leukemia, Lymphoid
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Chronic Myelogenous Leukemia
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Leukemia, Myeloid, Accelerated Phase
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Leukemia, Myelomonocytic, Acute
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Leukostasis
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Li-Fraumeni Syndrome
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Limb-Mammary Syndrome
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Lipodystrophy
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Lipodystrophy, Familial Partial
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Lissencephaly, X-Linked, 2
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Liver Diseases
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Furlong Syndrome
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Lower Extremity Deformities, Congenital
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Lubs X-Linked Mental Retardation Syndrome
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Lujan Fryns Syndrome
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Lung Diseases
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Lung Diseases, Obstructive
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Lymphangioleiomyomatosis
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Lymphatic Metastasis
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Lymphedema
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Lymphoma, Mantle-Cell
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Lymphoma, Non-Hodgkin
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Lymphoma, T-Cell, Peripheral
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Lynch Syndrome Ii
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Age-Related Macular Degeneration
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Maturity-Onset Diabetes Of The Young, Type 4
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