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236200
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HOMOCYSTINURIA
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Nevi and Melanomas
Melanoma
Neoplasms by Site
Digestive System Neoplasms
Pancreatic Neoplasms
Endocrine Gland Neoplasms
Pancreatic Neoplasms
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Marfan Syndrome
Bone Diseases, Metabolic
Osteoporosis
Spinal Diseases
Digestive System Diseases
Digestive System Neoplasms
Pancreatic Neoplasms
Liver Diseases
Fatty Liver
Pancreatic Diseases
Cystic Fibrosis
Pancreatic Neoplasms
Pancreatitis
Respiratory Tract Diseases
Lung Diseases
Cystic Fibrosis
Pleural Diseases
Pneumothorax
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Homocystinuria
Phenylketonurias
Brain Edema
Cerebrovascular Disorders
Intracranial Embolism and Thrombosis
Intracranial Thrombosis
Sinus Thrombosis, Intracranial
Stroke
Epilepsy
Seizures
Nervous System Malformations
Neural Tube Defects
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Down Syndrome
Seizures
Eye Diseases
Eye Abnormalities
Ectopia Lentis
Eye Diseases, Hereditary
Retinitis Pigmentosa
Lens Diseases
Lens Subluxation
Ectopia Lentis
Ocular Hypertension
Glaucoma
Refractive Errors
Myopia
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Pregnancy Complications
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Heart Diseases
Heart Defects, Congenital
Marfan Syndrome
Myocardial Ischemia
Coronary Disease
Coronary Artery Disease
Coronary Stenosis
Coronary Restenosis
Myocardial Infarction
Vascular Diseases
Aneurysm
Aneurysm, Ruptured
Aortic Rupture
Aortic Aneurysm
Aortic Rupture
Aortic Diseases
Aortic Aneurysm
Aortic Rupture
Arterial Occlusive Diseases
Arteriosclerosis
Coronary Artery Disease
Cerebrovascular Disorders
Intracranial Embolism and Thrombosis
Intracranial Thrombosis
Sinus Thrombosis, Intracranial
Stroke
Embolism and Thrombosis
Thromboembolism
Intracranial Embolism and Thrombosis
Intracranial Thrombosis
Sinus Thrombosis, Intracranial
Thrombosis
Thromboembolism
Intracranial Embolism and Thrombosis
Intracranial Thrombosis
Sinus Thrombosis, Intracranial
Venous Thrombosis
Thrombophlebitis
Myocardial Ischemia
Coronary Disease
Coronary Artery Disease
Coronary Stenosis
Coronary Restenosis
Myocardial Infarction
Peripheral Vascular Diseases
Phlebitis
Thrombophlebitis
Vasculitis
Phlebitis
Thrombophlebitis
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Factor VII Deficiency
Coagulation Protein Disorders
Factor VII Deficiency
Blood Protein Disorders
Hypoproteinemia
Hemorrhagic Disorders
Factor VII Deficiency
Thrombophilia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Down Syndrome
Marfan Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Chromosome Disorders
Down Syndrome
Eye Abnormalities
Ectopia Lentis
Nervous System Malformations
Neural Tube Defects
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Factor VII Deficiency
Chromosome Disorders
Down Syndrome
Cystic Fibrosis
Eye Diseases, Hereditary
Retinitis Pigmentosa
Marfan Syndrome
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Hyperhomocysteinemia
Homocystinuria
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Homocystinuria
Phenylketonurias
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Infant, Newborn, Diseases
Cystic Fibrosis
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Homocystinuria
Marfan Syndrome
Skin Diseases
Pigmentation Disorders
Hypopigmentation
Skin Diseases, Papulosquamous
Psoriasis
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Homocystinuria
Phenylketonurias
Malabsorption Syndromes
Hyperhomocysteinemia
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Hyperhomocysteinemia
Homocystinuria
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Homocystinuria
Phenylketonurias
Renal Tubular Transport, Inborn Errors
Renal Aminoacidurias
Cystinuria
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin B Deficiency
Folic Acid Deficiency
Hyperhomocysteinemia
Endocrine System Diseases
Endocrine Gland Neoplasms
Pancreatic Neoplasms
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Acute Disease
Disease Susceptibility
Genetic Predisposition to Disease
Postoperative Complications
Signs and Symptoms
Body Weight
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Seizures
Pain
Abdominal Pain
Signs and Symptoms, Digestive
Abdominal Pain
Wounds and Injuries
Rupture
Aortic Rupture
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