All terms in DOID
| Label | Id | Description |
|---|---|---|
| gene_cassette_member | SO_0005848 | |
| member_of_regulon | SO_1001217 | |
| gene_subarray_member | SO_0005849 | |
| mesoderm | UBERON_0000926 | |
| germ layer | UBERON_0000923 | |
| endoderm | UBERON_0000925 | |
| ectoderm | UBERON_0000924 | |
| anovulation | DOID_3781 | [An ovarian disease that is characterized by the absence of ovulation.] |
| central retinal vein occlusion | DOID_2450 | |
| retinal vein occlusion | DOID_1727 | |
| germ layer / neural crest | UBERON_0010316 | |
| protein S deficiency | DOID_2451 | |
| thrombophilia | DOID_2452 | |
| blood coagulation disease | DOID_1247 | |
| Coffin-Lowry syndrome | DOID_3783 | [A syndrome that is characterized by skeletal malformations, growth retardation, hearing deficit, paroxysmal movement disorders, and cognitive impairment in affected males and some carrier females, and has_material_basis_in mutation in the RSK2 gene on chromosome Xp22.] |
| angular blepharoconjunctivitis | DOID_2455 | [A blepharoconjunctivitis that is characterized by fissuring, scaling, maceration and erythema of the lateral or medial canthal area.] |
| blepharoconjunctivitis | DOID_2456 | [A blepharitis that is characterized by the dual combination of conjunctivitis with blepharitis.] |
| blepharitis | DOID_9423 | [An eyelid disease that is characterized by often chronic inflammation of the eyelid, generally the part where eyelashes grow.] |
| giant papillary conjunctivitis | DOID_2457 | |
| papillary conjunctivitis | DOID_2458 |