Liver Cirrhosis, Experimental
|
Prostatic Neoplasms
|
Breast Carcinoma
|
Drug-Induced Liver Injury
|
Hepatocellular Carcinoma
|
Diabetes Mellitus, Experimental
|
Obesity
|
Hypertension
|
Stomach Neoplasms
|
Autism
|
Colorectal Cancer
|
Heart Failure
|
Lung Neoplasms
|
Colonic Neoplasm
|
Disease Progression
|
Endometriosis
|
Reperfusion Injury
|
Osteoarthritis
|
Dermatitis, Contact
|
Esophageal Neoplasms
|
Diabetes Mellitus, Type 2
|
Acute Kidney Injury
|
Parkinson's Disease
|
Urinary Bladder Neoplasms
|
Neoplasms
|
Cholestasis
|
Drug-Related Side Effects And Adverse Reactions
|
Schizophrenia
|
Fatty Liver
|
Alzheimer's Disease
|
Cardiomyopathies
|
Adenocarcinoma
|
Carcinoma
|
Neoplasm Invasiveness
|
Esophageal Squamous Cell Carcinoma
|
Melanoma
|
Intellectual Disability
|
Kidney Failure, Chronic
|
Neoplasm Metastasis
|
Male Infertility
|
Nervous System Diseases
|
Neurodegenerative Diseases
|
Rheumatoid Arthritis
|
Kidney Disease
|
Myocardial Ischemia
|
Necrosis
|
Atherosclerosis
|
Precancerous Conditions
|
Osteoporosis
|
Anoxia
|
Mammary Neoplasms, Experimental
|
Weight Gain
|
Asthma
|
Carcinoma, Non-Small-Cell Lung
|
Renal Cell Carcinoma
|
Cardiac Hypertrophy
|
Liver Cirrhosis
|
Liver Diseases
|
Nerve Degeneration
|
Seizures
|
Brain Ischemia
|
Enterocolitis, Necrotizing
|
Parkinsonian Disorders
|
Leigh Disease
|
Squamous Cell Carcinoma
|
Stroke
|
Liver Neoplasms, Experimental
|
Inflammation
|
Mammary Neoplasms, Animal
|
Myocardial Infarction
|
Cell Transformation, Neoplastic
|
Liver Neoplasms
|
Hyperalgesia
|
Diabetes Mellitus, Type 1
|
Status Epilepticus
|
Diabetes Mellitus
|
Chronic Obstructive Pulmonary Disease
|
Hyperglycemia
|
Unipolar Depression
|
Autism Spectrum Disorder
|
Arthritis, Juvenile
|
Ischemia
|
Mitochondrial Complex I Deficiency
|
Insulin Resistance
|
Acute Lymphoblastic Leukemia
|
Neoplasm Recurrence, Local
|
Skin Diseases
|
Cardiovascular Disease
|
Epilepsy
|
Amphetamine-Related Disorders
|
Fibrosis
|
Myocardial Reperfusion Injury
|
Glioma
|
Pulmonary Hypertension
|
Mouth Neoplasms
|
Drug Eruptions
|
Psoriasis
|
Polycystic Ovary Syndrome
|
Pheochromocytoma
|
Dermatitis, Allergic Contact
|
Heart Diseases
|
Hyperthyroidism
|
Lymphoma, Large B-Cell, Diffuse
|
Stomach Ulcer
|
Major Depression
|
Lung Diseases
|
Colitis
|
Endometrial Neoplasm
|
Thrombosis
|
Hyperinsulinism
|
Dilated Cardiomyopathy
|
Meningomyelocele
|
Alcoholic Liver Cirrhosis
|
Turner Syndrome
|
Fever
|
Drug Dependence
|
Acute Coronary Syndrome
|
Asphyxia Neonatorum
|
Marfan Syndrome
|
Manganese Poisoning
|
Amyotrophic Lateral Sclerosis
|
Hepatitis, Chronic
|
Infertility, Female
|
Hypotension
|
Adenomatous Polyposis Coli
|
Cholangiocarcinoma
|
Hepatolenticular Degeneration
|
Down Syndrome
|
Peripheral Neuropathy
|
Osteosarcoma
|
Abortion, Spontaneous
|
Neural Tube Defects
|
Leukemia, Myeloid, Acute
|
Occupational Diseases
|
Adrenal Hyperplasia, Congenital
|
Brain Injuries
|
Vascular Diseases
|
Adenoma
|
Ovarian Neoplasms
|
Mesothelioma, Malignant
|
Respiratory Distress Syndrome, Adult
|
Edema
|
Mesothelioma
|
Carcinoma, Squamous Cell Of Head And Neck
|
Leukemia, Promyelocytic, Acute
|
Carcinoma, Adenoid Cystic
|
Endotoxemia
|
Lung Injury
|
Maple Syrup Urine Disease
|
Asbestosis
|
Carcinoma, Transitional Cell
|
Metabolism, Inborn Errors
|
Micronuclei, Chromosome-Defective
|
Fetal Growth Retardation
|
Mitochondrial Diseases
|
Mitochondrial Encephalomyopathies
|
Amenorrhea
|
Amino Acid Metabolism, Inborn Errors
|
Amyotrophic Lateral Sclerosis 1
|
Autoimmune Disease
|
Anemia
|
Neural Tube Defect, Folate-Sensitive
|
Glucose Intolerance
|
Neuroblastoma
|
Anemia, Hemolytic
|
2-Hydroxyglutaricaciduria
|
Cognitive Impairment
|
Granulomatous Disease, Chronic
|
Optic Atrophy, Hereditary, Leber
|
Bipolar Disorder
|
Ovarian Cysts
|
Pancreatic Carcinoma
|
Papilloma
|
Paranoid Disorders
|
Bone Diseases, Metabolic
|
Hemolysis
|
Coronary Artery Disease
|
Hepatic Encephalopathy
|
Hepatitis C
|
Preeclampsia
|
Albuminuria
|
Premature Birth
|
Huntington Disease
|
Protein Deficiency
|
Proteinuria
|
Brain Diseases
|
Pulmonary Embolism
|
Aortic Diseases
|
Pulmonary Fibrosis
|
Alcohol Dependence
|
Hypercholesterolemia
|
Hyperemia
|
Radiation Injuries, Experimental
|
Renal Insufficiency
|
Retinal Degeneration
|
Cone-Rod Dystrophy 2
|
Hyperplasia
|
Hypertension, Essential
|
Diabetic Angiopathies
|
Diabetic Nephropathy
|
Skin Neoplasms
|
Androgenetic Alopecia
|
Infarction, Middle Cerebral Artery
|
Keloid
|
Kidney Neoplasms
|
Ureteral Calculi
|
Drug Hypersensitivity
|
Burns
|
Learning Disorders
|
Arthritis, Experimental
|
Chronic Lymphocytic Leukemia
|
Hypercalcemia
|
Deficiency Diseases
|
Lipid Metabolism, Inborn Errors
|
Lymphoma, Follicular
|
Pyruvate Dehydrogenase Complex Deficiency Disease
|
Urticaria
|
Q Fever
|
Pancreatitis
|
Wounds And Injuries
|
Hearing Loss
|
Leukemia, Myeloid
|
Hyperhomocysteinemia
|
Head And Neck Neoplasms
|
Blood Coagulation Disorders
|
Growth Disorders
|
End Stage Liver Disease
|
Graves Ophthalmopathy
|
Retinal Diseases
|
Oral Submucous Fibrosis
|
Systemic Lupus Erythematosus
|
Anemia, Megaloblastic
|
Optic Atrophies, Hereditary
|
Ophthalmoplegia, Chronic Progressive External
|
Oligodendroglioma
|
Diabetes Complications
|
Venous Thrombosis
|
Gestational Diabetes
|
Allergy
|
Schistosomiasis Mansoni
|
Cocaine Dependence
|
Cleft Lip
|
Enchondromatosis
|
Abruptio Placentae
|
Sepsis
|
Sexual Dysfunctions, Psychological
|
Non-Alcoholic Fatty Liver Disease
|
Neutropenia
|
Neurotoxicity Syndromes
|
Chondroma
|
Nephrotic Syndrome
|
Nephrosis
|
Duodenal Ulcer
|
Primary Biliary Cirrhosis
|
Brain Neoplasms
|
Nephritis, Interstitial
|
Hypoglycemia
|
Glaucoma, Primary Open Angle
|
Dyskinesia, Drug-Induced
|
Hypogonadism
|
Hypopituitarism
|
Barrett's Esophagus
|
Genetic Predisposition To Disease
|
Hypothermia
|
Lewy Body Dementia
|
Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form
|
Ichthyosis, Lamellar
|
Spinocerebellar Ataxia 17
|
Immunoblastic Lymphadenopathy
|
Limb Dystonia
|
Intracerebral Hemorrhage
|
Muscular Diseases
|
Multiple Myeloma
|
Asthma, Occupational
|
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
|
Flushing
|
Mouth Diseases
|
Motor Neuron Disease
|
Disease Models, Animal
|
Cardiomyopathy, Hypertrophic
|
Fetal Alcohol Spectrum Disorders
|
Fatty Liver, Alcoholic
|
Intestinal Perforation
|
Intestinal Polyps
|
Thrombocytopenia
|
Thrombophilia
|
Methylmalonic Acidemia
|
Iron Metabolism Disorders
|
Thyroid Diseases
|
Iron Overload
|
Methemoglobinemia
|
Thyroid Carcinoma
|
Ischemic Attack, Transient
|
Tongue Neoplasms
|
Acidosis, Lactic
|
Embryo Loss
|
Keratosis
|
Hepatitis B
|
Kidney Stone
|
Lung Adenocarcinoma
|
Hyperphenylalaninemia, Bh4-Deficient, C
|
Bone Neoplasms
|
Hepatitis
|
Cortisone Reductase Deficiency
|
Porphyria Cutanea Tarda
|
Coumarin Resistance
|
Hemorrhage
|
Coronary Heart Disease
|
Mental Retardation, X-Linked
|
Mental Disorders
|
Leukoencephalopathies
|
Prenatal Exposure Delayed Effects
|
Prenatal Injuries
|
Creutzfeldt Jacob Disease
|
Critical Illness
|
Melas Syndrome
|
Cryptorchidism
|
Bradycardia
|
Peroxisomal Disorders
|
Arsenic Poisoning
|
Medulloblastoma
|
Lipidoses
|
Hemochromatosis
|
Psychoses, Substance-Induced
|
Hemangioma
|
Adrenoleukodystrophy
|
Pulmonary Edema
|
Carcinoma, Ductal, Breast
|
Lymphoma, T-Cell, Peripheral
|
Lymphoma, Non-Hodgkin
|
Pseudovaginal Perineoscrotal Hypospadias
|
Puberty, Precocious
|
Pulmonary Emphysema
|
Purine-Pyrimidine Metabolism, Inborn Errors
|
Pyloric Stenosis, Infantile Hypertrophic 1
|
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
|
Pyridoxine-Dependent Epilepsy
|
Pyruvate Metabolism, Inborn Errors
|
Radiation Injuries
|
Refsum Disease
|
Chronic Kidney Disease
|
Reticulocytosis
|
Retinal Detachment
|
Retinal Dystrophies
|
Retinitis Pigmentosa 10
|
Rhizomelic Chondrodysplasia Punctata, Type 3
|
Rickets
|
Rigid Spine Syndrome
|
Saccharopinuria
|
Sarcoidosis
|
Sarcosinemia
|
Schistosomiasis
|
Scrapie
|
Segawa Syndrome, Autosomal Recessive
|
Sexual Infantilism
|
Sezary Syndrome
|
Shock, Cardiogenic
|
Shock, Hemorrhagic
|
Septic Shock
|
Short Chain Acyl Coa Dehydrogenase Deficiency
|
Silicosis
|
Simpson-Golabi-Behmel Syndrome
|
Sinus Thrombosis, Intracranial
|
Sjogren-Larsson Syndrome
|
Skin Abnormalities
|
Sleep Deprivation
|
Smith-Lemli-Opitz Syndrome
|
Spasms, Infantile
|
Spastic Paraplegia, Hereditary
|
Spastic Paraplegia 5a, Autosomal Recessive
|
Spherocytosis, Hereditary
|
Spinal Cord Diseases
|
Spinal Cord Injuries
|
Splenic Diseases
|
Splenomegaly
|
Starvation
|
Toxic Epidermal Necrolysis
|
Subarachnoid Hemorrhage
|
Substance Withdrawal Syndrome
|
Succinic Semialdehyde Dehydrogenase Deficiency
|
Sulfite Oxidase Deficiency
|
Tachycardia, Sinus
|
Tachycardia, Ventricular
|
Takayasu Arteritis
|
Thyroid Carcinoma, Anaplastic
|
Thyroid Dyshormonogenesis 2a
|
Thyroid Dyshormonogenesis 4
|
Thyrotoxicosis
|
Torsades De Pointes
|
Trauma, Nervous System
|
Tremor
|
Trichuriasis
|
Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency
|
Trimethylaminuria
|
Tumor Lysis Syndrome
|
Tyrosinemias
|
Uremia
|
Urinary Bladder Neck Obstruction
|
Urinary Tract Infections
|
Urination Disorders
|
Urologic Neoplasms
|
Uterine Cervical Neoplasms
|
Uveitis
|
Vascular System Injuries
|
Ventricular Dysfunction
|
Ventricular Dysfunction, Left
|
Ventricular Premature Complexes
|
Ventricular Remodeling
|
Vestibular Diseases
|
Vitamin D Hydroxylation-Deficient Rickets, Type 1a
|
Vitamin D Hydroxylation-Deficient Rickets, Type 1b
|
Vlcad Deficiency
|
Weight Loss
|
Xanthinuria, Type I
|
Xanthomatosis, Cerebrotendinous
|
17-Hydroxysteroid Dehydrogenase Deficiency
|
Zellweger Syndrome
|
18-Hydroxylase Deficiency
|
2,4-Dienoyl-Coa Reductase Deficiency
|
2-Methylbutyryl-Coa Dehydrogenase Deficiency
|
3b-Hydroxysteroid Dehydrogenase Deficiency
|
3-Hydroxyacyl-Coa Dehydrogenase Deficiency
|
46, Xy Disorders Of Sex Development
|
Abnormalities, Drug-Induced
|
Acatalasia
|
Acidemia, Isovaleric
|
Acute Lung Injury
|
Acyl-Coa Dehydrogenase Family, Member 9, Deficiency Of
|
Adenocarcinoma Of Esophagus
|
Adrenal Gland Neoplasms
|
Adrenal Hyperplasia 2
|
Adrenal Hyperplasia, Congenital, Type 5
|
Adrenal Insufficiency
|
Adrenocortical Carcinoma
|
Agranulocytosis
|
Albinism Ocular Late Onset Sensorineural Deafness
|
Albinism, Oculocutaneous
|
Alexander Disease
|
Alkaptonuria
|
Alopecia Areata
|
Alopecia Universalis
|
Alpha-Ketoglutarate Dehydrogenase Deficiency
|
Alveolitis, Extrinsic Allergic
|
Anemia, Hemolytic, Congenital Nonspherocytic
|
Anemia, Iron-Deficiency
|
Sickle Cell Anemia
|
Anemia, Sideroblastic
|
Antisocial Personality Disorder
|
Antley-Bixler Syndrome Phenotype
|
Anxiety Disorder
|
Aortic Rupture
|
Aortic Valve Insufficiency
|
Apparent Mineralocorticoid Excess
|
Aromatase Deficiency
|
Cardiac Arrhythmia
|
Arteriosclerosis
|
Arteritis
|
Psoriatic Arthritis
|
Aspirin Induced Asthma
|
Ataxia
|
Atrial Fibrillation
|
Atrichia With Papular Lesions
|
Atrophy
|
Attention Deficit Hyperactivity Disorder
|
Basal Ganglia Diseases
|
Behcet's Syndrome
|
Beta-Thalassemia
|
Bile Acid Synthesis Defect, Congenital, 1
|
Bile Acid Synthesis Defect, Congenital, 2
|
Blood Coagulation Disorders, Inherited
|
Body Weight
|
Bone Diseases
|
Bone Fragility With Contractures, Arterial Rupture, And Deafness
|
Bone Marrow Diseases
|
Bone Resorption
|
Brain Diseases, Metabolic
|
Brain Edema
|
Brain Infarction
|
Bronchial Diseases
|
Bronchial Hyperreactivity
|
Bruck Syndrome 2
|
Brugada Syndrome 2
|
Brunner Syndrome
|
Burns, Chemical
|
Cachexia
|
Cadmium Poisoning
|
Carbon Tetrachloride Poisoning
|
Basal Cell Carcinoma
|
Carcinoma In Situ
|
Carcinoma, Intraductal, Noninfiltrating
|
Carcinoma, Lewis Lung
|
Carcinoma, Medullary
|
Cardiovascular Abnormalities
|
Carney-Stratakis Syndrome
|
Carotid Artery Diseases
|
Catalepsy
|
Cataract
|
Cataract And Cardiomyopathy
|
Central Nervous System Diseases
|
Cerebellar Diseases
|
Cerebral Infarction
|
Cervical Intraepithelial Neoplasia
|
Chloracne
|
Sclerosing Cholangitis
|
Choroideremia
|
Chromosome Breakage
|
Clubfoot
|
Ulcerative Colitis
|
Coloboma
|
Colonic Polyps
|
Coma
|
Congenital Adrenal Hyperplasia Due To 21 Hydroxylase Deficiency
|
Congenital Hemidysplasia With Ichthyosiform Erythroderma And Limb Defects
|
Congenital Hypothyroidism
|
Coproporphyria, Hereditary
|
Coronary Restenosis
|
Coronary Vasospasm
|
Cowden-Like Syndrome
|
Cutis Laxa
|
Cutis Laxa, Autosomal Recessive, Type Iib
|
Cyanosis
|
Dementia
|
Dermatitis, Irritant
|
Dermatitis, Occupational
|
Desmosterolosis
|
Diabetic Neuropathies
|
Diabetic Retinopathy
|
Dihydropyrimidine Dehydrogenase Deficiency
|
Dimethylglycine Dehydrogenase Deficiency
|
Disease Susceptibility
|
Disorders Of Sex Development
|
Dopamine Beta Hydroxylase Deficiency
|
Drug Metabolism, Poor, Cyp2c19-Related
|
Drug Metabolism, Poor, Cyp2d6-Related
|
Dyskinesias
|
Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency
|
Dystonic Disorders
|
Ehlers-Danlos Syndrome Type 6
|
Emphysema
|
Epilepsy, Idiopathic Generalized
|
Epilepsy, Temporal Lobe
|
Epilepsy, Tonic-Clonic
|
Erectile Dysfunction
|
Erythrocytosis, Familial, 3
|
Esophageal Stenosis
|
Esophagitis
|
Ethylmalonic Encephalopathy
|
Exfoliation Syndrome
|
Eye Diseases
|
Factor 8 Deficiency, Acquired
|
Familial Apoceruloplasmin Deficiency
|
Fanconi Syndrome
|
Farber Lipogranulomatosis
|
Favism
|
Fetal Nutrition Disorders
|
Folic Acid Deficiency
|
Fractures, Closed
|
Friedreich Ataxia
|
Friedreich Ataxia 1
|
Fundus Albipunctatus
|
Gait Disorders, Neurologic
|
Gallstones
|
Gastroesophageal Reflux
|
Gastrointestinal Diseases
|
Gastroparesis
|
Gaucher Disease
|
Ghosal Hematodiaphyseal Dysplasia
|
Glaucoma 1, Open Angle, A
|
Glaucoma 3, Primary Congenital, A
|
Open-Angle Glaucoma
|
Gliosarcoma
|
Focal Segmental Glomerulosclerosis
|
Glucosephosphate Dehydrogenase Deficiency
|
Glutaric Acidemia I
|
Goiter
|
Gonadal Dysgenesis Xx Type Deafness
|
Gout
|
Gout, Hprt-Related
|
Graft Vs Host Disease
|
Granuloma, Respiratory Tract
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative
|
Granulomatous Disease, Chronic, X-Linked
|
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death
|
Hamartoma
|
Hawkinsinuria
|
Hearing Loss, Sudden
|
Heart Defects, Congenital
|
Heart Injuries
|
Heavy Metal Toxicity
|
Hematologic Diseases
|
Hemolytic-Uremic Syndrome
|
Hemophilia A
|
Hepatitis, Animal
|
Hepatomegaly
|
Hepatorenal Syndrome
|
Hernia, Diaphragmatic
|
Hodgkins Lymphoma
|
Homocystinuria
|
Homocystinuria-Megaloblastic Anemia Due To Defect In Cobalamin Metabolism, Cble Complementation Type
|
Hydronephrosis
|
Hydroxyacyl-Coa Dehydrogenase, Type 2, Deficiency
|
Hyperaldosteronism
|
Hyperammonemia
|
Hypercalciuria
|
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant
|
Hyperglycinemia, Nonketotic
|
Hyperinsulinemic Hypoglycemia, Familial, 4
|
Hyperinsulinemic Hypoglycemia, Familial, 6
|
Hyperkalemia
|
Hyperkinesis
|
Hyperlipidemias
|
Hyperlysinemias
|
Hyperoxia
|
Hyperprolinemia Type 2
|
Hypertension, Malignant
|
Hypertension, Portal
|
Hypertension, Pregnancy-Induced
|
Hypertension, Renovascular
|
Hyperthyroxinemia
|
Hypertrophy
|
Hyperuricemia
|
Hypoaldosteronism
|
Hypospadias
|
Hypoxia-Ischemia, Brain
|
Inflammatory Bowel Disease
|
Intestinal Diseases
|
Isobutyryl-Coa Dehydrogenase Deficiency
|
Kidney Tubular Necrosis, Acute
|
Kyphosis
|
Lactate Dehydrogenase Deficiency Type A
|
Lameness, Animal
|
Language Development Disorders
|
Laryngeal Neoplasms
|
Lathosterolosis
|
Leber Congenital Amaurosis
|
Leber Congenital Amaurosis 13
|
Leber Congenital Amaurosis 3
|
Leiomyosarcoma
|
Visceral Leishmaniasis
|
Leukemia
|
Leukemia, Erythroblastic, Acute
|
Chronic Myelogenous Leukemia
|
Leukopenia
|
Leukoplakia, Oral
|
Lipoid Congenital Adrenal Hyperplasia
|
Liposarcoma
|
Liver Failure
|
Liver Failure, Acute
|
Long Qt Syndrome
|
Interstitial Lung Disease
|
Lymphatic Metastasis
|
Lymphoma
|
Lymphoma, B-Cell
|
Malaria
|
Malnutrition
|
Marie Unna Congenital Hypotrichosis
|
Marijuana Dependence
|
Mastocytosis, Systemic
|
Maxillofacial Abnormalities
|
Medium Chain Acyl Coa Dehydrogenase Deficiency
|
Memory Disorders
|
Menkes Kinky Hair Syndrome
|
Mental Retardation, X-Linked 17
|
Mental Retardation, X-Linked 3
|
Mental Retardation, X-Linked, Syndromic 10
|
Mental Retardation, X-Linked, Syndromic, Jarid1c-Related
|
Metabolic Diseases
|
Metabolic Syndrome X
|
Methylenetetrahydrofolate Reductase Deficiency
|
Methylmalonic Acidemia With Homocystinuria
|
Microsatellite Instability
|
Microvascular Angina
|
Mineralocorticoid Excess Syndrome, Apparent
|
Mitochondrial Complex Ii Deficiency
|
Mitochondrial Myopathies
|
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
|
Morphine Dependence
|
Mucositis
|
Multiple Chemical Sensitivity
|
Multiple Organ Failure
|
Multiple Sulfatase Deficiency Disease
|
Muscle Hypotonia
|
Muscle Rigidity
|
Muscular Atrophy
|
Muscular Dystrophies
|
Mycoplasma Infections
|
Myelodysplastic Syndromes
|
Myeloperoxidase Deficiency
|
Myocardial Stunning
|
Myoglobinuria
|
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay
|
Myopia
|
Nadh Cytochrome B5 Reductase Deficiency
|
Nasopharyngeal Carcinoma
|
Neoplasms, Experimental
|
Nephrolithiasis
|
Nervous System Malformations
|
Neuropathic Pain
|
Neurobehavioral Manifestations
|
Neurogenic Inflammation
|
Nevo Syndrome
|
Obesity, Abdominal
|
Oculocutaneous Albinism Type 1
|
Oculocutaneous Albinism Type 1b
|
Oculocutaneous Albinism Type 3
|
Oligomenorrhea
|
Oliguria
|
Opioid-Related Disorders
|
Optic Atrophy
|
Orofacial Cleft 1
|
Osteoarthropathy, Primary Hypertrophic
|
Osteogenesis Imperfecta
|
Osteogenesis Imperfecta, Type Viii
|
Osteoporosis, Postmenopausal
|
Ovarian Diseases
|
Ovarian Epithelial Cancer
|
Pancreatic Diseases
|
Pancytopenia
|
Paraganglioma
|
Paratuberculosis
|
Parkinson Disease 4, Autosomal Dominant Lewy Body
|
Pasteurellaceae Infections
|
Pediatric Obesity
|
Pentosuria
|
Peptic Ulcer Hemorrhage
|
Pericardial Effusion
|
Peripheral Vascular Diseases
|
Peroxisomal Acyl-Coa Oxidase Deficiency
|
Peters Anomaly
|
Phagocyte Bactericidal Dysfunction
|
Pharyngeal Neoplasms
|
Phencyclidine Abuse
|
Phobic Disorders
|
Phosphoglycerate Dehydrogenase Deficiency
|
Plaque, Amyloid
|
Pneumonia
|
Pneumonia, Aspiration
|
Poisoning
|
Polymyositis
|
Porphyria, South African Type
|
Pregnancy Complications
|
Primary Hyperoxaluria Type 2
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Primary Ovarian Insufficiency
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Progeria
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Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5
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Prostatic Hyperplasia
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