|
basilar artery occlusion
|
DOID_13446 |
|
|
obsolete streptococcal pharyngitis
|
DOID_12115 |
[A commensal streptococcal infectious disease that involves infection of the pharynx and sometimes the larynx and tonsils. It is caused by Group A Streptococcus bacteria. The common symptoms include fever, sore throat, headache, stomach ache, nausea, or chills.] |
|
angioimmunoblastic T-cell lymphoma
|
DOID_0111147 |
[A peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis.] |
|
glanders
|
DOID_13444 |
[A primary bacterial infectious disease that results in septicemic infection, has_material_basis_in Burkholderia mallei, which is transmitted by contact with tissues or body fluids of infected animals, or through mucosal surfaces such as the eyes and nose. The infection has symptom fever, has symptom chills, has symptom sweating, has symptom muscle aches, has symptom chest pain, has symptom muscle tightness, has symptom headache, has symptom mucopurulent nasal discharge, and has symptom nodular lesions in the lungs.] |
|
obsolete nerve deafness
|
DOID_12113 |
|
|
ureteropelvic junction obstruction
|
DOID_0111145 |
[A urinary tract obstruction characterized by a blockage at the renal pelvis where the kidney attaches to the ureter.] |
|
cartilage-hair hypoplasia
|
DOID_14773 |
[An ectodermal dysplasia characterized by short-limbed short stature and fine, sparse hair that has_material_basis_in homozygous or compound heterozygous mutation in the RMRP gene on chromosome 9p13.3.] |
|
acquired von Willebrand syndrome
|
DOID_0111146 |
[A blood coagulation disease characterized by development of a defect in clotting in the absence of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age. Typically this develops secondarily to other disorders, such as lymphoproliferative, myeloproliferative, cardiovascular and autoimmune disorders.] |
|
Rhinocladiella mackenziei
|
NCBITaxon_86056 |
|
|
Fonsecaea compacta
|
NCBITaxon_86057 |
|
|
Fonsecaea
|
NCBITaxon_40354 |
|
|
gonococcal bursitis
|
DOID_13453 |
[A bursitis that is characterized by an inflammation of a bursa caused by the Neisseria gonorrhoeae bacteria, resulting from gonorrhea that has spread to other parts of the body.] |
|
obsolete secondary syphilitic periostitis
|
DOID_12121 |
|
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scleritis
|
DOID_13452 |
|
|
pulmonary alveolar proteinosis
|
DOID_12120 |
[A lung disease that is characterized by abnormal accumulation of surfactant occurs within the alveoli, interfering with gas exchange.] |
|
obsolete Fryns syndrome
|
DOID_14787 |
|
|
susceptibility to acute lymphoblastic leukemia 3
|
MIM_615545 |
|
|
coccidioidomycosis
|
DOID_13450 |
[A primary systemic mycosis that results_in systemic fungal infection, has_material_basis_in Coccidioides immitis, transmitted_by airborne spores and has_symptom conjunctivitis, has_symptom arthritis, has_symptom chest pain and results_in_formation_of skin nodules.] |
|
spondyloepiphyseal dysplasia congenita
|
DOID_14789 |
[A spondyloepiphyseal dysplasia characterized by disproportionate short stature (short trunk), abnormal epiphyses, and flattened vertebral bodies that has_material_basis_in heterozygous mutation in the COL2A1 gene on chromosome 12q13.11.] |
|
autosomal dominant sensory ataxia 1
|
DOID_0111170 |
[A hereditary ataxia characterized by gait difficulty and instability especially in dark conditions resulting from sensory loss in the extremities and without cerebellar involvement that has_material_basis_in heterozygous mutations in the RNF170 gene on chromosome 8.] |