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166600
OPTA2
OSTEOPETROSIS, AUTOSOMAL DOMINANT 2
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Osteosclerosis
Osteopetrosis
Bone Resorption
Stomatognathic Diseases
Mouth Diseases
Facial Paralysis
Nervous System Diseases
Neurologic Manifestations
Paralysis
Facial Paralysis
Sensation Disorders
Vision Disorders
Blindness
Eye Diseases
Retinal Diseases
Retinal Degeneration
Vision Disorders
Blindness
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Signs and Symptoms
Neurologic Manifestations
Paralysis
Facial Paralysis
Sensation Disorders
Vision Disorders
Blindness
Wounds and Injuries
Fractures, Bone
Fractures, Spontaneous
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