Gendoo - MeSH tree view

MeSH Treeview

Query OMIM entry list

605361	SCA14	SPINOCEREBELLAR ATAXIA 14

→ High-scoring List

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Genetic Diseases, Inborn

Heredodegenerative Disorders, Nervous System

Spinocerebellar Degenerations

Spinocerebellar Ataxias

Pathological Conditions, Signs and Symptoms

Pathological Conditions, Anatomical

Muscular Atrophy

Pathologic Processes

Disease Attributes

Disease Susceptibility

Genetic Predisposition to Disease

Signs and Symptoms

Neurologic Manifestations

Cerebellar Ataxia

Neuromuscular Manifestations

Muscular Atrophy

Database Center for Life Science