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213010
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CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZ SYNDROME AND MECKEL SYNDROME
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Craniofacial Dysostosis
Hypertelorism
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Hypertelorism
Limb Deformities, Congenital
Digestive System Diseases
Liver Diseases
Nervous System Diseases
Nervous System Malformations
Neural Tube Defects
Encephalocele
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Eye Diseases
Eye Abnormalities
Coloboma
Eyelid Diseases
Blepharoptosis
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Polycystic Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Kidney Diseases, Cystic
Polycystic Kidney Diseases
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Heart Defects, Congenital
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Eye Abnormalities
Coloboma
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Hypertelorism
Limb Deformities, Congenital
Nervous System Malformations
Neural Tube Defects
Encephalocele
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hernia
Encephalocele
Pathologic Processes
Disease
Syndrome
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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