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120150
COL1A1
COLLAGEN, TYPE I, ALPHA-1
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Virus Diseases
RNA Virus Infections
Retroviridae Infections
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Connective Tissue
Neoplasms, Fibrous Tissue
Fibrosarcoma
Dermatofibrosarcoma
Sarcoma
Fibrosarcoma
Dermatofibrosarcoma
Neoplasms by Site
Skin Neoplasms
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Hyperostosis, Cortical, Congenital
Osteogenesis Imperfecta
Bone Diseases, Metabolic
Osteoporosis
Osteoporosis, Postmenopausal
Hyperostosis
Hyperostosis, Cortical, Congenital
Joint Diseases
Hip Dislocation, Congenital
Musculoskeletal Abnormalities
Hip Dislocation, Congenital
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Otosclerosis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
Carotid Artery Diseases
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Eye Diseases
Ocular Hypertension
Male Urogenital Diseases
Urogenital Abnormalities
Nephritis, Hereditary
Urologic Diseases
Kidney Diseases
Nephritis
Nephritis, Hereditary
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Nephritis, Hereditary
Urologic Diseases
Kidney Diseases
Nephritis
Nephritis, Hereditary
Pregnancy Complications
Fetal Death
Cardiovascular Diseases
Heart Diseases
Heart Valve Diseases
Aortic Valve Insufficiency
Vascular Diseases
Aneurysm
Aneurysm, Dissecting
Cerebrovascular Disorders
Carotid Artery Diseases
Hemostatic Disorders
Ehlers-Danlos Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
Hemostatic Disorders
Ehlers-Danlos Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Hip Dislocation, Congenital
Skin Abnormalities
Ehlers-Danlos Syndrome
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Urogenital Abnormalities
Nephritis, Hereditary
Genetic Diseases, Inborn
Osteogenesis Imperfecta
Skin Diseases, Genetic
Ehlers-Danlos Syndrome
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Infant, Newborn, Diseases
Hyperostosis, Cortical, Congenital
Infant, Premature, Diseases
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Ehlers-Danlos Syndrome
Epidermolysis Bullosa Dystrophica
Nephritis, Hereditary
Osteogenesis Imperfecta
Skin Diseases
Skin Abnormalities
Ehlers-Danlos Syndrome
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Skin Diseases, Genetic
Ehlers-Danlos Syndrome
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Skin Diseases, Vesiculobullous
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Skin Neoplasms
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Breakage
Ring Chromosomes
Translocation, Genetic
Death
Fetal Death
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Recurrence
Hemorrhage
Ossification, Heterotopic
Signs and Symptoms
Body Weight
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Wounds and Injuries
Back Injuries
Spinal Injuries
Spinal Fractures
Fractures, Bone
Fractures, Spontaneous
Spinal Fractures
Spinal Injuries
Spinal Fractures
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