MeSH Treeview
Query OMIM entry list
607932
MCOPS6
MICROPHTHALMIA, SYNDROMIC 6
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Synostosis
Craniosynostoses
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Micrognathism
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Micrognathism
Mouth Diseases
Mouth Abnormalities
Cleft Palate
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Mouth Abnormalities
Cleft Palate
Nervous System Diseases
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
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
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Mouth Abnormalities
Cleft Palate
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Infant, Newborn, Diseases
Infant, Premature, Diseases
Endocrine System Diseases
Thyroid Diseases
Hypothyroidism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
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