MeSH Treeview
Query OMIM entry list
277470
-
PONTOCEREBELLAR HYPOPLASIA, TYPE 2
→
High-scoring List
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Multiple System Atrophy
Olivopontocerebellar Atrophies
Cerebellar Diseases
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Movement Disorders
Multiple System Atrophy
Olivopontocerebellar Atrophies
Spinal Cord Diseases
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Multiple System Atrophy
Olivopontocerebellar Atrophies
Olivopontocerebellar Atrophies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Olivopontocerebellar Atrophies
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Disease
Syndrome
Database Center for Life Science
