MeSH Treeview
Query OMIM entry list
300032
ATRX
ATR-X GENE
→
High-scoring List
Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Musculoskeletal Diseases
Foot Deformities
Foot Deformities, Congenital
Clubfoot
Hand Deformities
Hand Deformities, Congenital
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Limb Deformities, Congenital
Lower Extremity Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Digestive System Diseases
Pancreatic Diseases
Cystic Fibrosis
Respiratory Tract Diseases
Lung Diseases
Cystic Fibrosis
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Damage, Chronic
Cerebral Palsy
Epilepsy
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Psychomotor Disorders
Paralysis
Paraplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Male Urogenital Diseases
Genital Diseases, Male
Testicular Diseases
Cryptorchidism
Urogenital Abnormalities
Cryptorchidism
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Pregnancy Complications
Fetal Death
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Thalassemia
alpha-Thalassemia
Bone Marrow Diseases
Myelodysplastic Syndromes
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Limb Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Hand Deformities, Congenital
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Urogenital Abnormalities
Cryptorchidism
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Thalassemia
alpha-Thalassemia
Cystic Fibrosis
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Infant, Newborn, Diseases
Cystic Fibrosis
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Endocrine System Diseases
Gonadal Disorders
Hypogonadism
Testicular Diseases
Cryptorchidism
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Death
Fetal Death
Disease
Syndrome
Growth Disorders
Signs and Symptoms
Body Weight
Overweight
Obesity
Failure to Thrive
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Paralysis
Paraplegia
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Database Center for Life Science
