|
coronary restenosis
|
DOID_4247 |
|
|
obsolete small intestinal gastrinoma
|
DOID_5578 |
|
|
Meesmann corneal dystrophy 2
|
DOID_0080671 |
[A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in heterozygous mutation in the KRT3 gene on chromosome 12q13.] |
|
Gerstmann-Straussler-Scheinker syndrome
|
DOID_4249 |
[A prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain.] |
|
B-lymphoblastic leukemia/lymphoma with BCR-ABL1
|
DOID_0080643 |
[A B-lymphoblastic leukemia/lymphoma that derives_from B-lymphoblasts and carries a translocation between the BCR gene on chromosome 22 and the ABL1 gene on chromosome 9. It results in the production of the p190 kd or p210 kd fusion protein.] |
|
B-lymphoblastic leukemia/lymphoma MLL rearranged
|
DOID_0080644 |
[A B-lymphoblastic leukemia/lymphoma that is characterized by the presence of lymphoblasts that carry a translocation between the KMT2A gene at 11q23.3 and another gene partner resulting in the production of a KMT2A related fusion protein.] |
|
B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1
|
DOID_0080645 |
[A B-lymphoblastic leukemia/lymphoma that is characterized by the presence of lymphoblasts that carry a translocation between the TEL gene on chromosome 12 and the AML1 gene on chromosome 21, (p13.2;q22.1). It results in the production of the TEL-AML1 (ETV6-RUNX1) fusion protein.] |
|
B-lymphoblastic leukemia/lymphoma with hyperdiploidy
|
DOID_0080646 |
[A B-lymphoblastic leukemia/lymphoma that is composed of B-lymphoblasts which contain more than 50 and usually less than 66 chromosomes.] |
|
isocyanates
|
CHEBI_53212 |
[Organonitrogen compounds that are derivatives of isocyanic acid; compounds containing the isocyanate functional group -N=C=O.] |
|
tongue carcinoma
|
DOID_0080641 |
[A tongue cancer that derives_from epithelial cells that cover the surface of the tongue.] |
|
tongue cancer
|
DOID_8649 |
|
|
Middle East respiratory syndrome
|
DOID_0080642 |
[A Coronavirus infectious disease that is characterized by severe respiratory illness, including fever, cough, and shortness of breath and that has_material_basis_in Middle East respiratory syndrome-related coronavirus (MERS-CoV, Betacoronavirus cameli).] |
|
Aplasia/Hypoplasia affecting the fundus
|
HP_0008057 |
|
|
B-lymphoblastic leukemia/lymphoma with hypodiploidy
|
DOID_0080647 |
[A B-lymphoblastic leukemia/lymphoma that is composed of B-lymphoblasts which contain less than 46 chromosomes.] |
|
B-lymphoblastic leukemia/lymphoma with IGH::IL3 fusion
|
DOID_0080648 |
[A B-lymphoblastic leukemia/lymphoma that is characterized by the presence of lymphoblasts that carry a translocation between the IL3 gene on chromosome 5 and the IGH locus on chromosome 14, (q31.1;q32.3).] |
|
B-lymphoblastic leukemia/lymphoma with TCF3-PBX1
|
DOID_0080649 |
[A B-lymphoblastic leukemia/lymphoma that is characterized by the presence of lymphoblasts that carry a translocation between the E2A gene on chromosome 19 and the PBX1 gene on chromosome 1.] |
|
Aplasia/Hypoplasia affecting the uvea
|
HP_0008055 |
|
|
Haemaphysalis concinna
|
NCBITaxon_523089 |
|
|
spinal cord primitive neuroectodermal neoplasm
|
DOID_6872 |
|
|
neuroectodermal tumor
|
DOID_171 |
|