All terms in DOID

Label Id Description
mature teratoma DOID_5566 [A teratoma that is composed exclusively of mature tissues derived from two or three germ layers.]
adult teratoma DOID_5565 [A benign teratoma that is present in an adult.]
benign teratoma DOID_0080602 [A germ cell benign neoplasm that derives_from mature tissue elements or a limited amount of immature tissue elements.]
obsolete malignant ovarian mixed epithelial neoplasm DOID_6899 [A mixed epithelial tumor of ovary that is cancerous.]
mediastinum teratoma DOID_5568 [A teratoma that is located_in the mediastinum.]
obsolete Malposition and malpresentation of fetus DOID_6897
alveolar soft part sarcoma DOID_4239 [A soft tissue cancer that is a slow growing tumor of an unknown origin that effects children and effects young adults.]
malignant syringoma DOID_5569
obsolete malignant soft tissue neoplasm of central nervous system DOID_4238
susceptibility to coronary heart disease 6 MIM_614466
Stickler syndrome 1 DOID_0080676 [A Stickler syndrome that has_material_basis_in heterozygous mutation in the COL2A1 gene on chromosome 12q13.]
otospondylomegaepiphyseal dysplasia, autosomal dominant DOID_0080677 [An osteochondrodysplasia that is characterized by by autosomal dominant inheritance of mutations in the COL11A2 gene.]
mucolipidosis III gamma DOID_0080678 [A mucolipidosis that is characterized by short stature, skeletal abnormalities, cardiomegaly, and developmental delay and that has_material_basis_in homozygous or compound heterozygous mutation in the GNPTG gene, which encodes the gamma subunit of N-acetylglucosamine-1-phosphotransferase, on chromosome 16p13.]
neuronal intestinal dysplasia type A DOID_0080679 [An intestinal pseudo-obstruction that is characterized by congenital hypoplasia or aplasia of the sympathetic innervation of the intestine.]
fibrochondrogenesis 1 DOID_0080672 [A fibrochondrogenesis that is characterized by a flat midface with a small nose and anteverted nares, significant shortening of all limb segments but relatively normal hands and feet, and a small bell-shaped thorax with a protuberant abdomen and that has_material_basis_in compound heterozygous mutation in the COL11A1 gene on chromosome 1p21.]
fibrochondrogenesis 2 DOID_0080673 [A fibrochondrogenesis that has_material_basis_in homozygous or heterozygous mutation in the COL11A2 gene on chromosome 6p21.3.]
luminal breast carcinoma B DOID_0080674 [A breast carcinoma that is characterized by low to moderate expression of genes characteristic of luminal epithelial cells including estrogen receptor (ER), and high expression of GGH, LAPTM4B, and CCNE1.]
Stickler syndrome 2 DOID_0080675 [A Stickler syndrome that has_material_basis_in heterozygous mutation in the COL11A1 gene on chromosome 1p21.]
excessive tearing SYMP_0019164
pustule SYMP_0019167 [A skin and integumentary tissue symptom that is characterized by a small circumscribed elevation of the skin containing pus and having an inflamed base.]