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Query OMIM entry list
601215
ATR
ATAXIA-TELANGIECTASIA AND RAD3-RELATED
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Muscle Tissue
Myosarcoma
Rhabdomyosarcoma
Sarcoma
Myosarcoma
Rhabdomyosarcoma
Neoplasms, Experimental
Neoplastic Processes
Cell Transformation, Neoplastic
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Dementia
Huntington Disease
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Spinal Cord Diseases
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurocutaneous Syndromes
Ataxia Telangiectasia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Ataxia Telangiectasia
Neurobehavioral Manifestations
Intellectual Disability
Williams Syndrome
Eye Diseases
Eye Abnormalities
Blepharophimosis
Eyelid Diseases
Blepharophimosis
Blepharoptosis
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Death
Cardiovascular Diseases
Heart Diseases
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Supravalvular
Williams Syndrome
Vascular Diseases
Telangiectasis
Ataxia Telangiectasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Williams Syndrome
Eye Abnormalities
Blepharophimosis
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Genetic Diseases, Inborn
Ataxia Telangiectasia
Chromosome Disorders
Williams Syndrome
Dwarfism
Heredodegenerative Disorders, Nervous System
Huntington Disease
Spinocerebellar Degenerations
Spinocerebellar Ataxias
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Ataxia Telangiectasia
Endocrine System Diseases
Dwarfism
Immune System Diseases
Immunologic Deficiency Syndromes
Ataxia Telangiectasia
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosomal Instability
Chromosome Fragility
Chromosome Breakage
Isochromosomes
Micronuclei, Chromosome-Defective
Translocation, Genetic
Death
Fetal Death
Disease
Syndrome
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Growth Disorders
Neoplastic Processes
Cell Transformation, Neoplastic
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Database Center for Life Science
