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 Categorias DeCS

C06 Digestive System Diseases .
C06.552 Liver Diseases .
C06.552.413 Hepatolenticular Degeneration .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10.228.140.079.493 Hepatolenticular Degeneration .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.360 Hepatolenticular Degeneration .
C10.228.140.380 Dementia .
C10.228.140.380.266 Frontotemporal Lobar Degeneration .
C10.228.140.380.266.299 Frontotemporal Dementia .
C10.228.662 Movement Disorders .
C10.228.662.400 Hepatolenticular Degeneration .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.487 Hepatolenticular Degeneration .
C10.574.950 TDP-43 Proteinopathies .
C10.574.950.300 Frontotemporal Lobar Degeneration .
C10.574.950.300.299 Frontotemporal Dementia .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.361 Hepatolenticular Degeneration .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.360 Hepatolenticular Degeneration .
C16.320.565.618 Metal Metabolism, Inborn Errors .
C16.320.565.618.403 Hepatolenticular Degeneration .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.360 Hepatolenticular Degeneration .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.360 Hepatolenticular Degeneration .
C18.452.648.618 Metal Metabolism, Inborn Errors .
C18.452.648.618.403 Hepatolenticular Degeneration .
C18.452.845 Proteostasis Deficiencies .
C18.452.845.800 TDP-43 Proteinopathies .
C18.452.845.800.300 Frontotemporal Lobar Degeneration .
C18.452.845.800.300.299 Frontotemporal Dementia .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.040 Acid Anhydride Hydrolases .
D08.811.277.040.025 Adenosine Triphosphatases .
D08.811.277.040.025.314 P-type ATPases .
D08.811.277.040.025.314.500 Copper-transporting ATPases .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.157 Carrier Proteins .
D12.776.157.530 Membrane Transport Proteins .
D12.776.157.530.450 Ion Pumps .
D12.776.157.530.450.250 Cation Transport Proteins .
D12.776.157.530.450.250.656 Copper-transporting ATPases .
D12.776.157.530.813 P-type ATPases .
D12.776.157.530.813.500 Copper-transporting ATPases .
D12.776.543 Membrane Proteins .
D12.776.543.585 Membrane Transport Proteins .
D12.776.543.585.450 Ion Pumps .
D12.776.543.585.450.250 Cation Transport Proteins .
D12.776.543.585.450.250.656 Copper-transporting ATPases .
D12.776.543.585.813 P-type ATPases .
D12.776.543.585.813.500 Copper-transporting ATPases .
F03 Mental Disorders .
F03.615 Neurocognitive Disorders .
F03.615.400 Dementia .
F03.615.400.380 Frontotemporal Lobar Degeneration .
F03.615.400.380.299 Frontotemporal Dementia .
 
 Termos
 Sinônimos e Históricos
Documentos
LILACS e MDL
 
Frontotemporal Dementia .
DDPAC .
Dementia, Frontotemporal .
Dementia, Frontotemporal, with Parkinsonism .
Dementia, Hereditary Dysphasic Disinhibition .
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex .
Disinhibition-Dementia-Parkinsonism-Amytrophy Complex .
FTD-GRN .
FTD-PGRN .
FTDP-17 .
FTLD with TDP-43 Pathology .
FTLD-17 GRN .
FTLD-TDP .
Familial Pick's Disease .
Frontotemporal Dementia with Parkinsonism .
Frontotemporal Dementia with Parkinsonism-17 .
Frontotemporal Dementia, Ubiquitin-Positive .
Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions .
Frontotemporal Lobe Dementia .
Frontotemporal Lobe Dementia (FLDEM) .
GRN-Related Frontotemporal Dementia .
HDDD1 .
HDDD2 .
Hereditary Dysphasic Disinhibition Dementia .
Multiple System Tauopathy with Presenile Dementia .
Semantic Dementia .
Wilhelmsen-Lynch Disease .
Complex, Disinhibition-Dementia-Parkinsonism-Amyotrophy .
Complex, Disinhibition-Dementia-Parkinsonism-Amytrophy .
Complices, Disinhibition-Dementia-Parkinsonism-Amyotrophy .
Complices, Disinhibition-Dementia-Parkinsonism-Amytrophy .
Dementia, Frontotemporal Lobe .
Dementia, Frontotemporal Lobe (FLDEM) .
Dementia, GRN-Related Frontotemporal .
Dementia, Semantic .
Dementia, Ubiquitin-Positive Frontotemporal .
Dementias, Frontotemporal .
Dementias, Frontotemporal Lobe .
Dementias, Frontotemporal Lobe (FLDEM) .
Dementias, GRN-Related Frontotemporal .
Dementias, Semantic .
Dementias, Ubiquitin-Positive Frontotemporal .
Disease, Familial Pick's .
Disease, Wilhelmsen-Lynch .
Diseases, Familial Pick's .
Diseases, Wilhelmsen-Lynch .
Disinhibition Dementia Parkinsonism Amyotrophy Complex .
Disinhibition Dementia Parkinsonism Amytrophy Complex .
Disinhibition-Dementia-Parkinsonism-Amyotrophy Complices .
Disinhibition-Dementia-Parkinsonism-Amytrophy Complices .
FTLD with TDP 43 Pathology .
Familial Pick Disease .
Familial Pick's Diseases .
Familial Picks Disease .
Frontotemporal Dementia with Parkinsonism 17 .
Frontotemporal Dementia, GRN-Related .
Frontotemporal Dementia, Ubiquitin Positive .
Frontotemporal Dementias .
Frontotemporal Dementias, GRN-Related .
Frontotemporal Dementias, Ubiquitin-Positive .
Frontotemporal Lobar Degeneration With Ubiquitin Positive Inclusions .
Frontotemporal Lobe Dementias .
Frontotemporal Lobe Dementias (FLDEM) .
GRN Related Frontotemporal Dementia .
GRN-Related Frontotemporal Dementias .
Lobe Dementia, Frontotemporal .
Lobe Dementias, Frontotemporal .
Pick's Disease, Familial .
Pick's Diseases, Familial .
Semantic Dementias .
Ubiquitin-Positive Frontotemporal Dementia .
Ubiquitin-Positive Frontotemporal Dementias .
Wilhelmsen Lynch Disease .
Wilhelmsen-Lynch Diseases .
1.00
 
Hepatolenticular Degeneration .
Copper Storage Disease .
Hepatic Form of Wilson Disease .
Hepato-Neurologic Wilson Disease .
Hepatocerebral Degeneration .
Hepatolenticular Degeneration Syndrome .
Kinnier-Wilson Disease .
Progressive Lenticular Degeneration .
Westphal-Strumpell Syndrome .
Wilson Disease, Hepatic Form .
Wilson's Disease .
Cerebral Pseudoscleroses .
Copper Storage Diseases .
Degeneration Syndrome, Hepatolenticular .
Degeneration Syndromes, Hepatolenticular .
Degeneration, Hepatocerebral .
Degeneration, Hepatolenticular .
Degeneration, Neurohepatic .
Degeneration, Progressive Lenticular .
Degenerations, Hepatocerebral .
Degenerations, Neurohepatic .
Disease, Copper Storage .
Diseases, Copper Storage .
Diseases, Hepato-Neurologic Wilson .
Diseases, Kinnier-Wilson .
Hepato Neurologic Wilson Disease .
Hepato-Neurologic Wilson Diseases .
Hepatocerebral Degenerations .
Hepatolenticular Degeneration Syndromes .
Kinnier Wilson Disease .
Kinnier-Wilson Diseases .
Lenticular Degeneration, Progressive .
Neurohepatic Degenerations .
Pseudoscleroses, Cerebral .
Pseudosclerosis, Cerebral .
Storage Disease, Copper .
Storage Diseases, Copper .
Syndrome, Hepatolenticular Degeneration .
Syndromes, Hepatolenticular Degeneration .
Westphal Strumpell Syndrome .
Westphal-Strumpell Syndromes .
Wilson Disease, Hepato-Neurologic .
Wilson Diseases, Hepato-Neurologic .
Wilsons Disease .
Wilson Disease .
Pseudosclerosis .
Cerebral Pseudosclerosis .
Neurohepatic Degeneration .
PROGRESSIVE LENTICULAR DEGENERATION .
WILSON'S DISEASE .
0.47
 
Copper-transporting ATPases .
ATP7A Protein .
ATP7B Cu-binding P type ATPase .
ATPase Copper Transporting alpha .
ATPase, Cu++ transporting, beta Polypeptide (Wilson Disease) .
Copper Pump 1 .
Copper-transporting ATPase .
Copper-transporting ATPase 1 .
Copper-transporting ATPase 2 .
Copper-transporting Adenosine Triphosphatases .
Cu(+)-transporting ATPases .
Cu-transporting ATPases .
Menkes Disease-associated Protein .
PINA Enzyme .
Pineal Night-specific ATPase .
Wilson Disease Cu-binding P Type ATPase .
Wilson Disease Protein .
ATP7B Cu binding P type ATPase .
ATPase 1, Copper-transporting .
ATPase, Copper-transporting .
ATPase, Pineal Night-specific .
ATPases, Copper-transporting .
ATPases, Cu-transporting .
Adenosine Triphosphatases, Copper-transporting .
Copper transporting ATPase .
Copper transporting ATPase 1 .
Copper transporting ATPase 2 .
Copper transporting ATPases .
Copper transporting Adenosine Triphosphatases .
Cu transporting ATPases .
Menkes Disease associated Protein .
Night-specific ATPase, Pineal .
Pineal Night specific ATPase .
Triphosphatases, Copper-transporting Adenosine .
Wilson Disease Cu binding P Type ATPase .
0.41