ITCMDBv1
DiseaseID 3288

淀粉样变性

disease

NCI2016_NCI-GLOSS_1602D:A group of diseases in which protein builds up in certain organs (localized amyloidosis) or throughout the body (systemic amyloidosis). Amyloidosis may be either primary (with no known cause), sec

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Disease: 1Symptom: 12Target: 27Links: 39
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Record Fields

Scalar fields from the final disease record.

Disease Id
3288
Core Entity Id
59475
Source Entity Count
2
Preferred Name
Amyloidosis
Name Cn
淀粉样变性
Name Pinyin
Dian Fen Yang Bian Xing
Name En
Amyloidosis
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Nutritional and Metabolic Diseases
Do Class
disease of metabolism
Hpo Class
Abnormality of metabolism/homeostasis
Mesh Class Name
Nutritional and Metabolic Diseases
Hpo Class Name
Abnormality of metabolism/homeostasis
Do Class Name
disease of metabolism
Disease Definition
NCI2016_NCI-GLOSS_1602D:A group of diseases in which protein builds up in certain organs (localized amyloidosis) or throughout the body (systemic amyloidosis). Amyloidosis may be either primary (with no known cause), secondary (caused by another disease, including some types of cancer, such as multiple myeloma), or hereditary (passed down from parents to children). Many organs are affected by amyloidosis. The organs affected may depend on whether the amyloidosis is the primary, secondary, or hereditary form.|NCI2016_CDISC_1602D:An accumulation of amyloid protein.|NCI2016_02D:A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.|MSH2017_2016_08_12:A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits.|MEDLINEPLUS_20151021:<p>Amyloidosis occurs when abnormal proteins called amyloids build up and form deposits. The deposits can collect in organs such as the kidney and heart. This can cause the organs to become stiff and unable to work the way they should. </p> <p>There are three main types of amyloidosis:</p> <ul> <li>Primary - with no known cause</li> <li>Secondary - caused by another disease, including some types of cancer</li> <li>Familial - passed down through genes</li> </ul> <p>Symptoms can vary, depending upon which organs are affected. Treatment depends on the type of amyloidosis you have. The goal is to help with symptoms and limit the production of proteins. If another disease is the cause, it needs to be treated.</p>|HPO2016_07_04:The presence of amyloid deposition in one or more tissues. Amyloidosis may be defined as the extracellular deposition of amyloid in one or more sites of the body. [HPO:probinson, pmid:21039326]|CSP2006:any disease manifested by the pathogenic accumulation of amyloid in organs and tissues.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.
Version
v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Amyloidosis
Role
preferred
Name
Amyloid Disease
Role
alias
Name
Amyloidosis, Unspecified
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Hpo
HP:0011034
Herb
HBDIS000132
Me Sh
D000686
Umls
C0002726
Icd10
E85E85.9
Sym Map
SMDE05799
Do Class
DOID:0014667
Dis Ge Net
C0002726
Umls Sty
T047
Hpo Class
HP:0001939
Me Sh Class
C18
Etcm Disease
Amyloidosis
Tcmbank Disease
102524398
Itcmdb Generated
ITX-DISEASE-11922DFBEE72ITX-DISEASE-4E74A80FB4DA

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Page Title
Disease Amyloidosis Details page
Do Class Name
disease of metabolism
Disease Type
disease
Hpo Class Name
Abnormality of metabolism/homeostasis
Do Disease Class
disease of metabolism
Hpo Disease Class
Abnormality of metabolism/homeostasis
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Amyloidosis
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Bone diseases;Immune diseases;Nephrological diseases;Neuronal diseases
Disease Definition
NCI2016_NCI-GLOSS_1602D:A group of diseases in which protein builds up in certain organs (localized amyloidosis) or throughout the body (systemic amyloidosis). Amyloidosis may be either primary (with no known cause), secondary (caused by another disease, including some types of cancer, such as multiple myeloma), or hereditary (passed down from parents to children). Many organs are affected by amyloidosis. The organs affected may depend on whether the amyloidosis is the primary, secondary, or hereditary form.|NCI2016_CDISC_1602D:An accumulation of amyloid protein.|NCI2016_02D:A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.|MSH2017_2016_08_12:A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits.|MEDLINEPLUS_20151021:<p>Amyloidosis occurs when abnormal proteins called amyloids build up and form deposits. The deposits can collect in organs such as the kidney and heart. This can cause the organs to become stiff and unable to work the way they should. </p> <p>There are three main types of amyloidosis:</p> <ul> <li>Primary - with no known cause</li> <li>Secondary - caused by another disease, including some types of cancer</li> <li>Familial - passed down through genes</li> </ul> <p>Symptoms can vary, depending upon which organs are affected. Treatment depends on the type of amyloidosis you have. The goal is to help with symptoms and limit the production of proteins. If another disease is the cause, it needs to be treated.</p>|HPO2016_07_04:The presence of amyloid deposition in one or more tissues. Amyloidosis may be defined as the extracellular deposition of amyloid in one or more sites of the body. [HPO:probinson, pmid:21039326]|CSP2006:any disease manifested by the pathogenic accumulation of amyloid in organs and tissues.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.|CHV2011_02:A group of diseases in which protein is deposited in specific organs or throughout the body.
Me Sh Disease Class
Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Nutritional and Metabolic Diseases
Umls Semantic Type Name
Disease or Syndrome