5 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: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:0080009 | X-linked dominant disease | A X-linked monogenic disease that has_material_basis_in dominant inheritance. |
DOID:0050735 | X-linked monogenic disease | A monogenic disease that has_material_basis_in mutations in genes on the X chromosome. |
58 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0080009 | DOID:0050437 |
is_a | DOID:0080009 | DOID:0050445 |
is_a | DOID:0080009 | DOID:0060316 |
is_a | DOID:0080009 | DOID:0060446 |
is_a | DOID:0080009 | DOID:0060450 |
is_a | DOID:0080009 | DOID:0060461 |
is_a | DOID:0080009 | DOID:0060599 |
is_a | DOID:0080009 | DOID:0060825 |
is_a | DOID:0080009 | DOID:0060848 |
is_a | DOID:0080009 | DOID:0060954 |
is_a | DOID:0080009 | DOID:0061015 |
is_a | DOID:0080009 | DOID:0070265 |
is_a | DOID:0080009 | DOID:0070380 |
is_a | DOID:0050735 | DOID:0080009 |
is_a | DOID:0050177 | DOID:0080009 |
is_a | DOID:630 | DOID:0080009 |
is_a | DOID:4 | DOID:0080009 |
is_a | DOID:0080009 | DOID:0080090 |
is_a | DOID:0080009 | DOID:0080352 |
is_a | DOID:0080009 | DOID:0080467 |
is_a | DOID:0080009 | DOID:0080470 |
is_a | DOID:0080009 | DOID:0080506 |
is_a | DOID:0080009 | DOID:0080509 |
is_a | DOID:0080009 | DOID:0080858 |
is_a | DOID:0080009 | DOID:0110030 |
is_a | DOID:0080009 | DOID:0110034 |
is_a | DOID:0080009 | DOID:0110058 |
is_a | DOID:0080009 | DOID:0110207 |
is_a | DOID:0080009 | DOID:0110209 |
is_a | DOID:0080009 | DOID:0110739 |