12 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:16 | integumentary system disease | A disease of anatomical entity that is located_in the integumentary system comprising the skin and its appendages. |
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:0080015 | physical disorder | A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. |
DOID:0050737 | autosomal recessive disease | An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop. |
DOID:4123 | nail disease | An integumentary system disease that is located_in nail. |
DOID:0080683 | nonsyndromic congenital nail disorder | A nail disease that is characterized by underdevelopment of nails. |
DOID:0080081 | nonsyndromic congenital nail disorder 3 | A nonsyndromic congenital nail disorder that is characterized by white discoloration of the nails. |
11 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0050736 | DOID:0080081 |
is_a | DOID:0080683 | DOID:0080081 |
is_a | DOID:0050737 | DOID:0080081 |
is_a | DOID:0050739 | DOID:0080081 |
is_a | DOID:7 | DOID:0080081 |
is_a | DOID:0050177 | DOID:0080081 |
is_a | DOID:0080015 | DOID:0080081 |
is_a | DOID:630 | DOID:0080081 |
is_a | DOID:4123 | DOID:0080081 |
is_a | DOID:4 | DOID:0080081 |
is_a | DOID:16 | DOID:0080081 |