All terms in DOID

Label Id Description
gingivitis DOID_3087
granulomatous orchitis DOID_3089
testicular disease DOID_2519
nervous system cancer DOID_3093 [An organ system cancer located_in the nervous system that affects the central or peripheral nervous system.]
obsolete neuroepithelial neoplasm DOID_3094
stenosis of lacrimal sac DOID_3096
lacrimal apparatus disease DOID_1400 [An eye disease that affects the lacrimal apparatus (the lacrimal gland and its related structures) which moisten and drain the eye.]
obsolete stenosis and insufficiency of lacrimal passage DOID_3097
small cell sarcoma DOID_3098 [A sarcoma characterized by the presence of small round or elongated malignant cells with a small amount of cytoplasm.]
familial erythrocytosis 1 DOID_0060652 [A primary polycythemia that has_material_basis_in mutation in the gene encoding the erythropoietin receptor. It is characterized by increased serum red blood cell mass and hemoglobin concentration, hypersensitivity of erythroid progenitors to EPO, and low serum levels of EPO.]
lethal congenital contracture syndrome 3 DOID_0060653 [A lethal congenital contracture syndrome that has_material_basis_in homozygous mutation in the PIP5K1C gene on chromosome 19p13.]
radius bone UBERON_0001423
forelimb long bone UBERON_0003607
radius endochondral element UBERON_0015001
forelimb zeugopod bone UBERON_0003466
lethal congenital contracture syndrome 4 DOID_0060654 [A lethal congenital contracture syndrome that has_material_basis_in homozygous mutation in the MYBPC1 gene on chromosome 12q23.]
autosomal recessive congenital ichthyosis DOID_0060655 [An ichthyosis that is characterized by autosomal recessive inheritance and abnormal skin scaling over the whole body due to a defect in keratinization.]
autosomal recessive congenital ichthyosis 1 DOID_0060656 [An autosomal recessive congenital ichthyosis that is characterized by lamellar ichthyosis, ectropion, eclabium and hyperkeratosis that has_material_basis_in homozygous or compound heterozygous mutation in the TGM1 gene on chromosome 14q11.2.]
regional part of cerebellar cortex UBERON_0002749
reticulohistiocytic granuloma DOID_4394