All terms in EFO
| Label | Id | Description |
|---|---|---|
| obsolete_congenital secondary polycythemia | Orphanet_238536 | |
| Bovine viral diarrhea virus 1 | NCBITaxon_11099 | |
| obsolete_metachromatic leukodystrophy, juvenile form | Orphanet_309263 | |
| obsolete_generalized peeling skin syndrome | Orphanet_263543 | |
| spondyloarthropathy | EFO_0000706 | [A group of inflammatory rheumatic diseases associated with arthritis and enthesitis, and often involving the axial skeleton. The most common form of spondyloarthritis is ankylosing spondylitis. Other forms include axial spondyloarthritis, peripheral spondyloarthritis, reactive arthritis, psoriatic arthritis/spondylitis and enteropathic arthritis/spondylitis., Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others.] |
| vertebral column structure | EFO_0001369 | [The post-cranial structural components forming the long axis of the vertebrate body; usually consists of the notochord, vertebrae, ribs, supraneurals, intermuscular bones, and unpaired median fins., The post-cranial structural components forming the long axis of the vertebrate body; in Danio, consisting of the notochord, vertebrae, ribs, supraneurals, intermuscular bones, and unpaired median fins.] |
| Myxococcus xanthus | NCBITaxon_34 | |
| West Nile virus | NCBITaxon_11082 | |
| Thin calvarium | HP_0010539 | [The presence of an abnormally thin calvarium.] |
| Yellow fever virus | NCBITaxon_11089 | |
| obsolete_peeling skin syndrome type A | Orphanet_263548 | |
| obsolete_Dianzani autoimmune lymphoproliferative disease | Orphanet_275523 | [Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly.] |
| obsolete_strain | EFO_0000710 | [A population or type of organisms that is geneticaly different from others of the same species and possessing a set of defined characteristics.] |
| obsolete_strain factor | EFO_0000711 | |
| obsolete_acral peeling skin syndrome | Orphanet_263534 | |
| Autoimmune lymphoproliferative syndrome with recurrent viral infections | Orphanet_275517 | [Autoimmune lymphoproliferative syndrome (ALPS) with recurrent viral infections is a rare genetic disorder characterized by lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses.] |
| Immunodeficiency syndrome with autoimmunity | Orphanet_169355 | |
| obsolete_Tay-Sachs disease, B1 variant | Orphanet_309239 | |
| Dengue virus 4 | NCBITaxon_11070 | |
| GM2-gangliosidosis, AB variant | Orphanet_309246 |