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300209
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SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2
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Musculoskeletal Diseases
Hand Deformities
Hand Deformities, Congenital
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Limb Deformities, Congenital
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Respiratory Tract Diseases
Ciliary Motility Disorders
Otorhinolaryngologic Diseases
Ciliary Motility Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Epilepsy, Generalized
Spasms, Infantile
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Limb Deformities, Congenital
Hand Deformities, Congenital
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Diseases in Twins
Signs and Symptoms
Edema
Hydrops Fetalis
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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