All terms in DOID

Label Id Description
Charcot-Marie-Tooth disease type 7 DOID_0080069 [A Charcot-Marie-Tooth disease that is characterized by optic atrophy followed by retinitis pigmentosa.]
susceptibility to X-linked autism 1 MIM_300425
obsolete breast arcinoma metastatic to the liver DOID_12724
obsolete lung carcinoma metastatic to the liver DOID_12723
sternum cancer DOID_5090 [A bone cancer and neoplasm of chest wall and sternal disorder that is located_in the sternum.]
obsolete liver metastasis DOID_12722
cerebral atherosclerosis DOID_12720
thoracic disease DOID_0060118 [A disease of anatomical entity that is located_in the thoracic cavity.]
obsolete transmissible gastroenteritis of swine DOID_5085 [A viral infectious disease that results_in inflammation located_in stomach and located_in intestine in pigs, has_material_basis_in Transmissible gastroenteritis virus, which is transmitted_by ingestion of food contaminated with feces. The infection has_symptom vomiting, has_symptom watery yellow diarrhea, has_symptom weight loss, and has_symptom dehydration.]
obsolete feline infectious peritonitis DOID_5087 [A viral infectious disease that results_in infection in cats, located_in peritoneum, has_material_basis_in Feline infectious peritonitis virus, which is transmitted_by contact with the infected cat, and transmitted_by congenital method. The infection has_symptom sneezing, has_symptom watery eyes, has_symptom nasal discharge, and has_symptom accumulation of fluid in the abdomen.]
obsolete transmissible enteritis of turkeys DOID_5086 [A viral infectious disease that results_in inflammation located_in intestine of turkeys, has_material_basis_in Turkey coronavirus, which is transmitted_by ingestion of food contaminated with feces, or transmitted_by fomites contaminated with feces. The infection has_symptom diarrhea, has_symptom anorexia, has_symptom decreased weight, and has_symptom depression.]
mixed epithelial stromal tumour DOID_5088
mixed cell type cancer DOID_154 [A cell type cancer that has_material_basis_in abnormally proliferating cells derives_from two germinal layers of tissue.]
obsolete retroverted incarcerated gravid uterus DOID_12727
autosomal recessive spinocerebellar ataxia 11 DOID_0080063 [An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the SYT14 gene on chromosome 1q32.]
Caroli syndrome DOID_0081394 [A syndrome that is characterized by the presence of associated congenital hepatic fibrosis and that is associated with autosomal recessive polycystic kidney disease.]
Morbillivirus NCBITaxon_11229
Harel-Yoon syndrome DOID_0081395 [A syndrome that is characterized by delayed psychomotor development, intellectual disability, truncal hypotonia, spasticity, and peripheral neuropathy and that has_material_basis_in heterozygous mutation in the ATAD3A gene on chromosome 1p36.]
autosomal recessive spinocerebellar ataxia 17 DOID_0080064 [An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24.]
neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome DOID_0081396 [A syndrome that is characterized in infants showing respiratory insufficiency and almost no spontaneous movement at birth, usually requiring mechanical ventilation and admission to the neonatal intensive care unit and that has_material_basis_in compound heterozygous mutation in the ATAD3A gene on chromosome 1p36.33.]