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Query OMIM entry list
611038
MCOP3
MICROPHTHALMIA, ISOLATED 3
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Synostosis
Craniosynostoses
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Eye Diseases
Eye Abnormalities
Anophthalmos
Microphthalmos
Eye Diseases, Hereditary
Retinitis Pigmentosa
Lens Diseases
Cataract
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Scleral Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Eye Abnormalities
Anophthalmos
Microphthalmos
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Infant, Newborn, Diseases
Infant, Premature, Diseases
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Diseases in Twins
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