MeSH Treeview
Query OMIM entry list
309530
MRX1
MENTAL RETARDATION, X-LINKED 1
→
High-scoring List
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Cerebellar Ataxia
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Learning Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Fragile X Syndrome
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosomal Instability
Chromosome Fragility
Sex Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Learning Disorders
Intellectual Disability
Database Center for Life Science