Gendoo - MeSH tree view

MeSH Treeview

Query OMIM entry list

606882	ATP7B	ATPase, Cu(2+)-TRANSPORTING, BETA POLYPEPTIDE

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Digestive System Diseases

Hepatitis, Animal

Hepatolenticular Degeneration

Cardiovascular Diseases

Vascular Diseases

Cerebrovascular Disorders

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Genetic Diseases, Inborn

Genetic Diseases, X-Linked

Mental Retardation, X-Linked

Menkes Kinky Hair Syndrome

Heredodegenerative Disorders, Nervous System

Hepatolenticular Degeneration

Menkes Kinky Hair Syndrome

Mental Retardation, X-Linked

Menkes Kinky Hair Syndrome

Metabolism, Inborn Errors

Brain Diseases, Metabolic, Inborn

Hepatolenticular Degeneration

Menkes Kinky Hair Syndrome

Metal Metabolism, Inborn Errors

Hepatolenticular Degeneration

Menkes Kinky Hair Syndrome

Skin and Connective Tissue Diseases

Menkes Kinky Hair Syndrome

Nutritional and Metabolic Diseases

Metabolic Diseases

Brain Diseases, Metabolic

Brain Diseases, Metabolic, Inborn

Hepatolenticular Degeneration

Menkes Kinky Hair Syndrome

Metabolism, Inborn Errors

Brain Diseases, Metabolic, Inborn

Hepatolenticular Degeneration

Menkes Kinky Hair Syndrome

Metal Metabolism, Inborn Errors

Hepatolenticular Degeneration

Menkes Kinky Hair Syndrome

Animal Diseases

Hepatitis, Animal

Pathological Conditions, Signs and Symptoms

Signs and Symptoms

Neurologic Manifestations

Gait Disorders, Neurologic

Neurobehavioral Manifestations

Communication Disorders

Language Disorders

Speech Disorders

Articulation Disorders

Database Center for Life Science