All terms in DOID

Label Id Description
bronchitis DOID_6132 [A bronchial disease that is an inflammation of the bronchial tubes. It is caused by bacteria and viruses. The disease has_symptom cough with mucus, has_symptom shortness of breath, has_symptom low fever and has_symptom chest tightness.]
childhood pleomorphic rhabdomyosarcoma DOID_7463
eye carcinoma in situ DOID_8792 [A carcinoma in situ that is characterized by the spread of cancer in the eye and the lack of invasion of surrounding tissues.]
spindle cell variant squamous cell breast carcinoma DOID_7460 [A breast squamous cell carcinoma that is characterized by the presence of spindle-shaped malignant cells and arises from the breast parenchyma.]
breast squamous cell carcinoma DOID_5514 [A breast metaplastic carcinoma that arises from squamous epithelial cells.]
large cell keratinizing variant squamous cell breast carcinoma DOID_7461 [A breast squamous cell carcinoma characterized by large epithelial cells that contain keratin.]
obsolete Hodgkin's lymphoma, mixed cellularity, involving spleen DOID_8798
solitary cyst of breast DOID_10349 [A breast cyst that is characterized by single, fluid-filled cyst in the breast parenchyma.]
breast cyst DOID_10350 [A breast benign neoplasm that is characterized by a fluid-filled sac.]
chronic NK-cell lymphocytosis DOID_7465 [A hypersensitivity reaction type IV disease that is characterized by absolute lymphocytosis of natural killer (CD3- CD16+) cells often with concurrent cytopenia and has_symptom fever, arthralgia, apthous ulcers, vasculitic skin rash, and peripheral neuropathy.]
obsolete Hodgkin's granuloma involving spleen DOID_8795
uterine corpus epithelioid leiomyosarcoma DOID_6139 [A uterus leiomyosarcoma characterized by the presence of round epithelioid, rhabdoid and large vacuolated cells intermingled with spindled cells and clear or eosinophilic cytoplasm.]
uterus leiomyosarcoma DOID_5289 [A uterine Corpus sarcoma and leiomyosarcoma and uterine Corpus smooth muscle neoplasm that is located_in the smooth muscle of the uterus.]
autosomal recessive nonsyndromic deafness 106 DOID_0080261 [An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the EPS8L2 gene on chromosome 11p15.]
autosomal recessive nonsyndromic deafness DOID_0050565 [A nonsyndromic deafness characterized by an autosomal recessive inheritance mode.]
autosomal recessive nonsyndromic deafness 107 DOID_0080262 [An autosomal recessive nonsyndromic deafness that has_material_basis_in compound heterozygous mutation in the WBP2 gene on chromosome 17q25.]
obsolete Spitz nevus DOID_7468
autosomal recessive nonsyndromic deafness 108 DOID_0080263 [An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the ROR1 gene on chromosome 1p31.]
obsolete balloon cell nevus DOID_7469
exudative vitreoretinopathy 7 DOID_0080264 [An exudative vitreoretinopathy that has_material_basis_in heterozygous mutation in the CTNNB1 gene on chromosome 3p22.1.]