01
Diseases
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
amyloidosis, hereditary, transthyretin-related
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
- Standard Disease Name
- amyloidosis, hereditary, transthyretin-related
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D004487
- OMIM ID
- MTHU037616
- UMLS ID
- C0151603
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NICHD_1602D:Profound accumulation of an excessive amount of fluid throughout the body.|NCI2016_02D:A condition that is characterized by the presence of generalized edema. Causes include congestive heart failure, liver failure, renal failure, and severe malnutrition.|HPO2016_07_04:An extreme form of generalized edema with widespread and massive edema due to effusion of fluid into the extracellular space. [HPO:probinson]
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Targets
target disease8 Targets
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06
PPP1R1A
protein phosphatase 1 regulatory inhibitor subunit 1A
protein phosphatase 1 regulatory inhibitor subunit 1A
07
08