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214150
COFS1
CEREBROOCULOFACIOSKELETAL SYNDROME 1
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Neoplasms
Precancerous Conditions
Xeroderma Pigmentosum
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Cockayne Syndrome
Osteochondrodysplasias
Osteosclerosis
Osteopetrosis
Bone Diseases, Metabolic
Osteoporosis
Spinal Diseases
Spinal Curvatures
Kyphosis
Foot Deformities
Foot Deformities, Congenital
Clubfoot
Jaw Diseases
Jaw Abnormalities
Micrognathism
Joint Diseases
Ankylosis
Arthrogryposis
Contracture
Muscular Diseases
Arthrogryposis
Contracture
Muscular Disorders, Atrophic
Muscular Dystrophies
Musculoskeletal Abnormalities
Arthrogryposis
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Micrognathism
Microcephaly
Limb Deformities, Congenital
Lower Extremity Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Micrognathism
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Micrognathism
Nervous System Diseases
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscular Atrophy
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Eye Diseases
Eye Abnormalities
Microphthalmos
Lens Diseases
Cataract
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Death
Fetal Diseases
Cardiovascular Diseases
Vascular Diseases
Hypotension
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cockayne Syndrome
Chromosome Disorders
Eye Abnormalities
Microphthalmos
Musculoskeletal Abnormalities
Arthrogryposis
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Micrognathism
Microcephaly
Limb Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Skin Abnormalities
Xeroderma Pigmentosum
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Micrognathism
Fetal Diseases
Genetic Diseases, Inborn
Chromosome Disorders
Dwarfism
Cockayne Syndrome
Heredodegenerative Disorders, Nervous System
Cockayne Syndrome
Muscular Dystrophies
Skin Diseases, Genetic
Xeroderma Pigmentosum
Skin and Connective Tissue Diseases
Skin Diseases
Photosensitivity Disorders
Xeroderma Pigmentosum
Pigmentation Disorders
Xeroderma Pigmentosum
Skin Abnormalities
Xeroderma Pigmentosum
Skin Diseases, Genetic
Xeroderma Pigmentosum
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Cockayne Syndrome
Xeroderma Pigmentosum
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Death
Fetal Death
Disease
Syndrome
Disease Attributes
Diseases in Twins
Growth Disorders
Signs and Symptoms
Failure to Thrive
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscular Atrophy
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