MeSH Treeview
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112240
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BONE FRAGILITY WITH CRANIOSYNOSTOSIS, OCULAR PROPTOSIS, HYDROCEPHALUS, AND DISTINCTIVE FACIAL FEATURES
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Synostosis
Craniosynostoses
Osteochondrodysplasias
Osteogenesis Imperfecta
Bone Diseases, Metabolic
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Tooth Diseases
Tooth Abnormalities
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Hydrocephalus
Intracranial Hypertension
Hydrocephalus
Eye Diseases
Eye Abnormalities
Orbital Diseases
Exophthalmos
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
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Stomatognathic System Abnormalities
Tooth Abnormalities
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Osteogenesis Imperfecta
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Osteogenesis Imperfecta
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Recurrence
Growth Disorders
Signs and Symptoms
Edema
Hydrops Fetalis
Wounds and Injuries
Fractures, Bone
Fractures, Spontaneous
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