11 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:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
DOID:75 | lymphatic system disease | An immune system disease that is located_in the lymphatic system. |
DOID:4977 | lymphedema | |
DOID:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
DOID:0050736 | autosomal dominant disease | An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. |
DOID:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
DOID:0050580 | hereditary lymphedema | A lymphedema commonly located_in legs, caused_by congenital abnormalities in the lymphatic system. |
DOID:0070211 | hereditary lymphedema IB | A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in the chromosomal region 6q16.2-q22.1. |
10 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0050580 | DOID:0070211 |
is_a | DOID:0050736 | DOID:0070211 |
is_a | DOID:4 | DOID:0070211 |
is_a | DOID:2914 | DOID:0070211 |
is_a | DOID:630 | DOID:0070211 |
is_a | DOID:0050739 | DOID:0070211 |
is_a | DOID:4977 | DOID:0070211 |
is_a | DOID:0050177 | DOID:0070211 |
is_a | DOID:75 | DOID:0070211 |
is_a | DOID:7 | DOID:0070211 |