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305450
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OPITZ-KAVEGGIA SYNDROME
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Craniofacial Dysostosis
Synostosis
Syndactyly
Spinal Diseases
Spinal Curvatures
Kyphosis
Scoliosis
Hand Deformities
Hand Deformities, Congenital
Joint Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Limb Deformities, Congenital
Syndactyly
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Synostosis
Syndactyly
Digestive System Diseases
Digestive System Abnormalities
Anus, Imperforate
Gastrointestinal Diseases
Esophageal Diseases
Deglutition Disorders
Esophageal Motility Disorders
Stomach Diseases
Gastric Outlet Obstruction
Pyloric Stenosis
Stomatognathic Diseases
Mouth Diseases
Mouth Abnormalities
Stomatognathic System Abnormalities
Mouth Abnormalities
Respiratory Tract Diseases
Respiration Disorders
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Nervous System Malformations
Neural Tube Defects
Arnold-Chiari Malformation
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Prader-Willi Syndrome
Williams Syndrome
Neuromuscular Manifestations
Muscle Hypotonia
Pain
Headache
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Death
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Cardiomegaly
Heart Defects, Congenital
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Supravalvular
Williams Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Prader-Willi Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Chromosome Disorders
Prader-Willi Syndrome
Sex Chromosome Disorders
Fragile X Syndrome
Williams Syndrome
Digestive System Abnormalities
Anus, Imperforate
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Limb Deformities, Congenital
Hand Deformities, Congenital
Syndactyly
Synostosis
Syndactyly
Nervous System Malformations
Neural Tube Defects
Arnold-Chiari Malformation
Stomatognathic System Abnormalities
Mouth Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Prader-Willi Syndrome
Sex Chromosome Disorders
Fragile X Syndrome
Williams Syndrome
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Fragile X Syndrome
Nutritional and Metabolic Diseases
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Choristoma
Hypertrophy
Cardiomegaly
Pathologic Processes
Chromosome Aberrations
Chromosome Inversion
Sex Chromosome Aberrations
Death
Fetal Death
Disease
Syndrome
Disease Attributes
Facies
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
Pain
Headache
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Pain
Headache
Signs and Symptoms, Digestive
Constipation
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