7 Parents
Identifier | Name | Description |
---|---|---|
DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
DOID:0014667 | disease of metabolism | A disease that involves errors in metabolic processes of building or degradation of molecules. |
DOID:18 | urinary system disease | A disease of anatomical entity that is located_in kidney, ureter, bladder and urethra. |
DOID:557 | kidney disease | A urinary system disease that is located_in the kidney. |
DOID:9120 | amyloidosis | A disease of metabolism that is characterized by extracellular tissue deposition of mis-folded amyloid fibrils built up by twisted protofilaments, deposited in the spaces between the cells of vital organs, causing disruption of organ tissue structure and function. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition. |
DOID:0080927 | apolipoprotein A-IV associated amyloidosis | An amyloidosis that is characterized by slowly progressive renal dysfunction, increased serum creatinine, mostly normal urine analysis with no significant proteinuria and associated heart disease. |
6 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:557 | DOID:0080927 |
is_a | DOID:9120 | DOID:0080927 |
is_a | DOID:0014667 | DOID:0080927 |
is_a | DOID:4 | DOID:0080927 |
is_a | DOID:18 | DOID:0080927 |
is_a | DOID:7 | DOID:0080927 |