MeSH Treeview
Query OMIM entry list
130100
EPS
ELASTOSIS PERFORANS SERPIGINOSA
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Osteogenesis Imperfecta
Digestive System Diseases
Liver Diseases
Hepatolenticular Degeneration
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Hepatolenticular Degeneration
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Movement Disorders
Hepatolenticular Degeneration
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hepatolenticular Degeneration
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Down Syndrome
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Insufficiency
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Cardiovascular Diseases
Vascular Diseases
Aneurysm
Aneurysm, Ruptured
Aortic Rupture
Aortic Aneurysm
Aortic Rupture
Aortic Diseases
Aortic Aneurysm
Aortic Rupture
Hemostatic Disorders
Ehlers-Danlos Syndrome
Pseudoxanthoma Elasticum
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
Hemostatic Disorders
Ehlers-Danlos Syndrome
Pseudoxanthoma Elasticum
Lymphatic Diseases
Lymphoproliferative Disorders
Granuloma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Down Syndrome
Chromosome Disorders
Down Syndrome
Skin Abnormalities
Ehlers-Danlos Syndrome
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Pseudoxanthoma Elasticum
Genetic Diseases, Inborn
Chromosome Disorders
Down Syndrome
Heredodegenerative Disorders, Nervous System
Hepatolenticular Degeneration
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Osteogenesis Imperfecta
Skin Diseases, Genetic
Cutis Laxa
Darier Disease
Ehlers-Danlos Syndrome
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Pseudoxanthoma Elasticum
Infant, Newborn, Diseases
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Ehlers-Danlos Syndrome
Necrobiotic Disorders
Granuloma Annulare
Osteogenesis Imperfecta
Cutis Laxa
Pseudoxanthoma Elasticum
Skin Diseases
Facial Dermatoses
Hair Diseases
Folliculitis
Keratosis
Darier Disease
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Leg Dermatoses
Necrobiotic Disorders
Granuloma Annulare
Skin Abnormalities
Ehlers-Danlos Syndrome
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Pseudoxanthoma Elasticum
Skin Diseases, Genetic
Cutis Laxa
Darier Disease
Ehlers-Danlos Syndrome
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Pseudoxanthoma Elasticum
Skin Diseases, Vesiculobullous
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hepatolenticular Degeneration
Metal Metabolism, Inborn Errors
Hepatolenticular Degeneration
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Disease
Syndrome
Disease Attributes
Chronic Disease
Fibrosis
Cicatrix
Granuloma
Granuloma Annulare
Wounds and Injuries
Rupture
Aortic Rupture
Database Center for Life Science
