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216550
COH1
COHEN SYNDROME
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Craniofacial Dysostosis
Synostosis
Syndactyly
Marfan Syndrome
Hand Deformities
Hand Deformities, Congenital
Muscular Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Microcephaly
Limb Deformities, Congenital
Syndactyly
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Synostosis
Syndactyly
Digestive System Diseases
Gastrointestinal Diseases
Esophageal Diseases
Deglutition Disorders
Esophageal Motility Disorders
Gastroesophageal Reflux
Stomatognathic Diseases
Mouth Diseases
Mouth Abnormalities
Stomatognathic System Abnormalities
Mouth Abnormalities
Tooth Abnormalities
Tooth Diseases
Malocclusion
Tooth Abnormalities
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
Intracranial Hemorrhages
Cerebral Hemorrhage
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Language Development Disorders
Learning Disorders
Intellectual Disability
Prader-Willi Syndrome
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Hypotonia
Muscular Atrophy
Sensation Disorders
Vision Disorders
Neuromuscular Diseases
Muscular Diseases
Eye Diseases
Eye Abnormalities
Eye Diseases, Hereditary
Retinitis Pigmentosa
Lens Diseases
Cataract
Refractive Errors
Myopia
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Retinal Detachment
Uveal Diseases
Choroid Diseases
Vision Disorders
Night Blindness
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Heart Diseases
Heart Defects, Congenital
Marfan Syndrome
Heart Valve Diseases
Heart Valve Prolapse
Mitral Valve Prolapse
Vascular Diseases
Cerebrovascular Disorders
Intracranial Hemorrhages
Cerebral Hemorrhage
Embolism and Thrombosis
Thrombosis
Venous Thrombosis
Thrombophlebitis
Peripheral Vascular Diseases
Phlebitis
Thrombophlebitis
Vasculitis
Phlebitis
Thrombophlebitis
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Leukocyte Disorders
Leukopenia
Agranulocytosis
Neutropenia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Marfan Syndrome
Prader-Willi Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Marfan Syndrome
Chromosome Disorders
Prader-Willi Syndrome
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Microcephaly
Limb Deformities, Congenital
Hand Deformities, Congenital
Syndactyly
Synostosis
Syndactyly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Stomatognathic System Abnormalities
Mouth Abnormalities
Tooth Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Prader-Willi Syndrome
Eye Diseases, Hereditary
Retinitis Pigmentosa
Marfan Syndrome
Metabolism, Inborn Errors
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Marfan Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Endocrine System Diseases
Gonadal Disorders
Puberty, Delayed
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Hernia
Hernia, Diaphragmatic
Hernia, Hiatal
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Diseases in Twins
Growth Disorders
Hemorrhage
Intracranial Hemorrhages
Cerebral Hemorrhage
Signs and Symptoms
Body Weight
Overweight
Obesity
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Language Development Disorders
Learning Disorders
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Hypotonia
Muscular Atrophy
Sensation Disorders
Vision Disorders
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