MeSH Treeview
Query OMIM entry list
103000
AK1
ADENYLATE KINASE 1
→
High-scoring List
Neoplasms
Hamartoma
Tuberous Sclerosis
Neoplasms, Multiple Primary
Tuberous Sclerosis
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Musculoskeletal Diseases
Joint Diseases
Nail-Patella Syndrome
Digestive System Diseases
Liver Diseases
Hepatomegaly
Nervous System Diseases
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Neurocutaneous Syndromes
Tuberous Sclerosis
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Tuberous Sclerosis
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Glucosephosphate Dehydrogenase Deficiency
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Nail-Patella Syndrome
Chromosome Disorders
Nervous System Malformations
Malformations of Cortical Development
Tuberous Sclerosis
Skin Abnormalities
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital Nonspherocytic
Glucosephosphate Dehydrogenase Deficiency
Chromosome Disorders
Heredodegenerative Disorders, Nervous System
Tuberous Sclerosis
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I
Nail-Patella Syndrome
Neoplastic Syndromes, Hereditary
Tuberous Sclerosis
Skin and Connective Tissue Diseases
Skin Diseases
Nail Diseases
Nail-Patella Syndrome
Skin Abnormalities
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Glucosephosphate Dehydrogenase Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I
Nutrition Disorders
Malnutrition
Deficiency Diseases
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Hepatomegaly
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosome Duplication
Trisomy
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Chronic Disease
Hyperbilirubinemia
Jaundice
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Signs and Symptoms, Respiratory
Anoxia
Skin Manifestations
Jaundice
Database Center for Life Science