MeSH Treeview
Query OMIM entry list
211900
HFTC
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL
→
High-scoring List
Parasitic Diseases
Helminthiasis
Nematode Infections
Secernentea Infections
Spirurida Infections
Filariasis
Onchocerciasis
Skin Diseases, Parasitic
Onchocerciasis
Neoplasms
Cysts
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Adipose Tissue
Lipoma
Neoplasms by Site
Digestive System Neoplasms
Pancreatic Neoplasms
Endocrine Gland Neoplasms
Pancreatic Neoplasms
Skin Neoplasms
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Hyperostosis, Cortical, Congenital
Hyperostosis
Hyperostosis, Cortical, Congenital
Joint Diseases
Muscular Diseases
Digestive System Diseases
Digestive System Neoplasms
Pancreatic Neoplasms
Gastrointestinal Diseases
Gastrointestinal Hemorrhage
Intestinal Diseases
Pancreatic Diseases
Pancreatic Neoplasms
Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Tooth Diseases
Tooth Abnormalities
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
Intracranial Arterial Diseases
Intracranial Aneurysm
Neuromuscular Diseases
Muscular Diseases
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Cardiovascular Diseases
Vascular Diseases
Aneurysm
Intracranial Aneurysm
Cerebrovascular Disorders
Intracranial Arterial Diseases
Intracranial Aneurysm
Hemostatic Disorders
Pseudoxanthoma Elasticum
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
Hemostatic Disorders
Pseudoxanthoma Elasticum
Lymphatic Diseases
Lymphoproliferative Disorders
Granuloma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Pseudoxanthoma Elasticum
Stomatognathic System Abnormalities
Tooth Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Lipidoses
Metal Metabolism, Inborn Errors
Hypophosphatemia, Familial
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Skin Diseases, Genetic
Pseudoxanthoma Elasticum
Infant, Newborn, Diseases
Hyperostosis, Cortical, Congenital
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Pseudoxanthoma Elasticum
Skin Diseases
Skin Abnormalities
Pseudoxanthoma Elasticum
Skin Diseases, Genetic
Pseudoxanthoma Elasticum
Skin Diseases, Infectious
Skin Diseases, Parasitic
Onchocerciasis
Skin Neoplasms
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Calcinosis
Lipid Metabolism Disorders
Lipidoses
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Lipidoses
Metal Metabolism, Inborn Errors
Hypophosphatemia, Familial
Renal Tubular Transport, Inborn Errors
Hypophosphatemia, Familial
Phosphorus Metabolism Disorders
Hypophosphatemia
Hypophosphatemia, Familial
Endocrine System Diseases
Endocrine Gland Neoplasms
Pancreatic Neoplasms
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Cysts
Pathologic Processes
Disease
Syndrome
Granuloma
Hemorrhage
Gastrointestinal Hemorrhage
Database Center for Life Science