serw-MX  [xml]  
 


    
 DeCS Categories

C04 Neoplasms .
C04.182 Cysts .
C04.182.089 Bone Cysts .
C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.070 Bone Cysts .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.736 Osteolysis, Essential .
C05.116.264 Bone Resorption .
C05.116.264.579 Osteolysis .
C05.116.264.579.704 Osteolysis, Essential .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.200 Fabry Disease .
C10.228.140.300 Cerebrovascular Disorders .
C10.228.140.300.275 Cerebral Small Vessel Diseases .
C10.228.140.300.275.374 Fabry Disease .
C14 Cardiovascular Diseases .
C14.907 Vascular Diseases .
C14.907.077 Angiomatosis .
C14.907.253 Cerebrovascular Disorders .
C14.907.253.329 Cerebral Small Vessel Diseases .
C14.907.253.329.374 Fabry Disease .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.124 Fabry Disease .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.200 Fabry Disease .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.300 Fabry Disease .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.200 Fabry Disease .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.200 Fabry Disease .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.300 Fabry Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.200 Fabry Disease .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.300 Fabry Disease .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.200 Fabry Disease .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Osteolysis, Essential .
Cystic Angiomatosis Of Bone, Diffuse .
Gorham-Stout Disease .
Bone Disease, Disappearing .
Essential Osteolyses .
Essential Osteolysis .
Idiopathic Multicentric Osteolyses .
Idiopathic Multicentric Osteolysis .
Massive Osteolyses .
Massive Osteolysis .
Multicentric Osteolyses, Idiopathic .
Multicentric Osteolysis, Idiopathic .
Osteolyses, Essential .
Osteolyses, Idiopathic Multicentric .
Osteolyses, Massive .
Disappearing Bone Disease .
Gorham Disease .
Osteolysis, Idiopathic Multicentric .
Osteolysis, Massive .
Syndromes of bone destruction where the cause is not obvious such as neoplasia, infection, or trauma. The destruction follows various patterns: massive (Gorham disease), multicentric (HAJDU-CHENEY SYNDROME), or carpal/tarsal. .
1.00
28691
 
Angiomatosis .
Angiomatoses .
A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic. .
0.56
772441
 
Fabry Disease .
Angiokeratoma Diffuse .
Angiokeratoma, Diffuse .
Ceramide Trihexosidase Deficiency .
Fabry's Disease .
GLA Deficiency .
Hereditary Dystopic Lipidosis .
alpha-Galactosidase A Deficiency .
alpha-Galactosidase A Deficiency Disease .
Anderson Fabry Disease .
Deficiency, Ceramide Trihexosidase .
Deficiency, GLA .
Deficiency, alpha-Galactosidase A .
Diffuse Angiokeratoma .
Lipidosis, Hereditary Dystopic .
alpha Galactosidase A Deficiency .
alpha Galactosidase A Deficiency Disease .
Angiokeratoma Corporis Diffusum .
Anderson-Fabry Disease .
An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. .
0.54
 
Bone Cysts .
Ganglia, Intra-Osseous .
Ganglion, Intra-Osseous .
Intra-Osseous Ganglia .
Intra-Osseous Ganglion .
Bone Cyst .
Cyst, Bone .
Cyst, Solitary .
Cyst, Subchondral .
Cysts, Bone .
Cysts, Solitary .
Cysts, Subchondral .
Ganglia, Intra Osseous .
Ganglias, Intra-Osseous .
Ganglias, Intraosseous .
Ganglion, Intra Osseous .
Ganglion, Intraosseous .
Ganglions, Intra-Osseous .
Intra Osseous Ganglia .
Intra Osseous Ganglion .
Intra-Osseous Ganglias .
Intra-Osseous Ganglions .
Intraosseous Ganglia .
Intraosseous Ganglias .
Intraosseous Ganglions .
Solitary Cyst .
Subchondral Cyst .
Subchondral Cysts .
Solitary Cysts .
Ganglia, Intraosseous .
Intraosseous Ganglion .
Benign unilocular lytic areas in the proximal end of a long bone with well defined and narrow endosteal margins. The cysts contain fluid and the cyst walls may contain some giant cells. Bone cysts usually occur in males between the ages 3-15 years. .
0.50
1523641