|
bullous keratopathy
|
DOID_11031 |
|
|
Graves' disease
|
DOID_12361 |
[An autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located_in thyroid gland.] |
|
obsolete meningococcal meningitis
|
DOID_9929 |
|
|
asphyxiating thoracic dystrophy 2
|
DOID_0110086 |
[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the IFT80 gene on chromosome 3q25.] |
|
lateral displacement of eye
|
DOID_12360 |
|
|
dermoid cyst of skin
|
DOID_13691 |
[A dermoid cyst that is located_in the skin.] |
|
arrhythmogenic right ventricular dysplasia 12
|
DOID_0110083 |
[An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the gene encoding junction plakoglobin (JUP) on chromosome 17q21.] |
|
acute gonococcal cystitis
|
DOID_13690 |
[An acute cystitis that is caused by gonorrhea.] |
|
arrhythmogenic right ventricular dysplasia 13
|
DOID_0110084 |
[An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the CTNNA3 gene on chromosome 10q21.] |
|
arrhythmogenic right ventricular dysplasia 10
|
DOID_0110081 |
[An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the desmoglein-2 gene (DSG2) on chromosome 18q12.] |
|
arrhythmogenic right ventricular dysplasia 11
|
DOID_0110082 |
[An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the desmocollin-2 gene (DSC2) on chromosome 18q.] |
|
trachea
|
UBERON_0003126 |
|
|
depersonalization disorder
|
DOID_11038 |
[A dissociative disorder in which the sufferer is affected by persistent or recurrent feelings of depersonalization and/or derealization.] |
|
skull
|
UBERON_0003129 |
|
|
subdivision of skeletal system
|
UBERON_0000075 |
|
|
prolapse of urethra
|
DOID_12369 |
[A prolapse of female genital organ that is characterized by the descent of the urethra from the normal anatomic location toward or through the vaginal opening.] |
|
chronic rapidly progressive glomerulonephritis
|
DOID_11036 |
|
|
dissociative amnesia
|
DOID_11037 |
[A dissociative disorder where he continuity of the patient's memory is disrupted. Patients with dissociative amnesia have recurrent episodes in which they forget important personal information or events, usually connected with trauma or severe stress.] |
|
contact lens corneal edema
|
DOID_11034 |
|
|
asphyxiating thoracic dystrophy 5
|
DOID_0110089 |
[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the WDR19 gene on chromosome 4p14.] |