7 Parents
Identifier | Name | Description |
---|---|---|
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:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
DOID:3211 | lysosomal storage disease | An inherited metabolic disorder that involve an abnormal accumulation of substances inside the lysosome resulting from defects in lysosomal function. |
DOID:655 | inherited metabolic disorder | A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality. |
DOID:9455 | lipid storage disease | A lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues. |
DOID:14503 | neuronal ceroid lipofuscinosis |
20 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:14503 | DOID:0110720 |
is_a | DOID:14503 | DOID:0110721 |
is_a | DOID:14503 | DOID:0110722 |
is_a | DOID:14503 | DOID:0110723 |
is_a | DOID:14503 | DOID:0110724 |
is_a | DOID:14503 | DOID:0110725 |
is_a | DOID:14503 | DOID:0110726 |
is_a | DOID:14503 | DOID:0110727 |
is_a | DOID:14503 | DOID:0110728 |
is_a | DOID:14503 | DOID:0110729 |
is_a | DOID:14503 | DOID:0110730 |
is_a | DOID:14503 | DOID:0110731 |
is_a | DOID:14503 | DOID:0110732 |
is_a | DOID:14503 | DOID:0110733 |
is_a | DOID:9455 | DOID:14503 |
is_a | DOID:630 | DOID:14503 |
is_a | DOID:655 | DOID:14503 |
is_a | DOID:3211 | DOID:14503 |
is_a | DOID:0014667 | DOID:14503 |
is_a | DOID:4 | DOID:14503 |