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261600
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PHENYLKETONURIA
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Bacterial Infections and Mycoses
Infection
Bone Diseases, Infectious
Osteomyelitis
Neoplasms
Neoplasms by Site
Digestive System Neoplasms
Liver Neoplasms
Liver Neoplasms, Experimental
Neoplasms, Experimental
Liver Neoplasms, Experimental
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Hyperostosis, Cortical, Congenital
Bone Diseases, Infectious
Osteomyelitis
Bone Diseases, Metabolic
Hyperostosis
Hyperostosis, Cortical, Congenital
Jaw Diseases
Jaw Abnormalities
Pierre Robin Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Microcephaly
Digestive System Diseases
Digestive System Neoplasms
Liver Neoplasms
Liver Neoplasms, Experimental
Liver Diseases
Hepatic Insufficiency
Liver Failure
Liver Neoplasms
Liver Neoplasms, Experimental
Pancreatic Diseases
Cystic Fibrosis
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Pierre Robin Syndrome
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Respiratory Tract Diseases
Lung Diseases
Cystic Fibrosis
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Phenylketonurias
Phenylketonuria, Maternal
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neural Tube Defects
Spinal Dysraphism
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Eye Diseases
Lens Diseases
Cataract
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Abortion, Spontaneous
Abortion, Habitual
Fetal Death
Fetal Diseases
Fetal Growth Retardation
Phenylketonuria, Maternal
Prenatal Injuries
Prenatal Exposure Delayed Effects
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Ductus Arteriosus, Patent
Heart Diseases
Heart Defects, Congenital
Ductus Arteriosus, Patent
Hemic and Lymphatic Diseases
Lymphatic Diseases
Lymphangiectasis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Ductus Arteriosus, Patent
Chromosome Disorders
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neural Tube Defects
Spinal Dysraphism
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Chromosome Disorders
Cystic Fibrosis
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Phenylketonurias
Phenylketonuria, Maternal
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Phenylketonurias
Phenylketonuria, Maternal
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Metal Metabolism, Inborn Errors
Hemochromatosis
Infant, Newborn, Diseases
Cystic Fibrosis
Hyperostosis, Cortical, Congenital
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Scleroderma, Localized
Skin Diseases
Scleroderma, Localized
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Phenylketonurias
Phenylketonuria, Maternal
Calcium Metabolism Disorders
Calcinosis
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Iron Metabolism Disorders
Iron Overload
Hemochromatosis
Lipid Metabolism Disorders
Lipidoses
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Phenylketonurias
Phenylketonuria, Maternal
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Phenylketonurias
Phenylketonuria, Maternal
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Metal Metabolism, Inborn Errors
Hemochromatosis
Endocrine System Diseases
Diabetes Mellitus
Diabetes Mellitus, Type 1
Immune System Diseases
Autoimmune Diseases
Diabetes Mellitus, Type 1
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Death
Fetal Death
Disease Attributes
Chronic Disease
Disease Susceptibility
Genetic Predisposition to Disease
Recurrence
Growth Disorders
Fetal Growth Retardation
Hemorrhage
Signs and Symptoms
Body Weight
Birth Weight
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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