Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
rete testis	UBERON_0003959
plexiform neurofibroma	DOID_5151
neurofibroma of gallbladder	DOID_5150
mediastinal melanocytic neurilemmoma	DOID_6484
bladder signet ring cell adenocarcinoma	DOID_6481
atypical neurofibroma	DOID_5153
lung acinar adenocarcinoma	DOID_6482
cellular neurofibroma	DOID_5152
multiple mucosal neuroma	DOID_5155
borna disease	DOID_5154	[A viral infectious disease that results_in infection, which affects dopaminergic neurotransmission located_in central nervous system, has_material_basis_in Borna disease virus, which is transmitted_by contact with infected oronasal secretions. The infection has_symptom mood disturbances, has_symptom behaviour disturbances, has_symptom cognitive disturbances, has_symptom neurologic disturbances, and has_symptom movement impairment.]
obsolete metastatic tumor to the iris	DOID_6488
reproductive system mucosa	UBERON_0019042
benign pleural mesothelioma	DOID_5157
pleural cancer	DOID_5158	[A connective tissue cancer that located_in the pleura.]
mitochondrial DNA depletion syndrome 12a	DOID_0080130	[A mitochondrial DNA depletion syndrome that is characterized by severe hypotonia due to mitochondrial dysfunction apparent at birth and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 25 member 4 gene on chromosome 4q35.]
periosteal osteogenic sarcoma	DOID_6489
mitochondrial DNA depletion syndrome 13	DOID_0080131	[A mitochondrial DNA depletion syndrome that is characterized by early infantile onset of encephalopathy, hypotonia, lactic acidosis, and severe global developmental delay, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the F-box and leucine-rich repeat protein 4 gene on chromosome 6q16.]
Sengers syndrome	DOID_0080132	[A mitochondrial DNA depletion syndrome that is characterized by congenital cataracts, hypertrophic cardiomyopathy, skeletal myopathy, exercise intolerance, and lactic acidosis, but normal mental development, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the acylglycerol kinase gene on chromosome 7q34.]
ring staphyloma	DOID_11594
scleral staphyloma	DOID_11595