All terms in DOID

Label Id Description
hypohidrosis DOID_11155 [A sweat gland disease that is characterized by reduced ability to sweat, has_symptom hyperthermia and dry skin of affected areas, and has_material_basis_in trauma to the sweat glands.]
chief cell of parathyroid gland CL_0000446
band keratopathy DOID_11164
Charcot-Marie-Tooth disease dominant intermediate B DOID_0110197 [A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in mutation in the gene encoding dynamin-2 (DNM2).]
common wart DOID_11165 [A viral infectious disease that results_in infection located_in skin, has_material_basis_in human papillomavirus (types 2 and 4). This infection is characterized by a raised wart with roughened surface, most common on hands, but can grow anywhere on the body.]
anterior spinal artery UBERON_0005431
Charcot-Marie-Tooth disease recessive intermediate C DOID_0110198 [A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in homozygous or compound heterozygous mutation in the PLEKHG5 gene on chromosome 1p36.]
Charcot-Marie-Tooth disease type 4E DOID_0110195 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or heterozygous mutation in the EGR2 gene on chromosome 10q21 or by heterozygous mutation in the MPZ gene on chromosome 1q23.]
obsolete apnea of prematurity DOID_11163
Charcot-Marie-Tooth disease type 4G DOID_0110196 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.]
Charcot-Marie-Tooth disease type 4F DOID_0110193 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13.]
neonatal respiratory failure DOID_11161 [A respiratory failure that is characterized by inadequate gas exchange by the respiratory system in neonates.]
Vagus nerve disease DOID_12491
Charcot-Marie-Tooth disease type 4B3 DOID_0110194 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SBF1 gene on chromosome 22q.]
Charcot-Marie-Tooth disease type 4B1 DOID_0110191 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the gene encoding the myotubularin-related protein-2 (MTMR2).]
Langerhans cell CL_0000453
Charcot-Marie-Tooth disease type 4H DOID_0110192 [A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutations in the gene encoding frabin (FGD4).]
clivus of occipital bone UBERON_0004108
anogenital venereal wart DOID_11168 [A viral infectious disease that results_in infection located_in skin of vagina, cervix, uterus, anus, penis, scrotum, mouth, or throat, has_material_basis_in human papillomaviruses (types 6 and 11), which are transmitted_by direct contact with the skin during oral, genital, or anal sex with an infected partner. The infection has_symptom anogenital warts.]
obsolete vaginal condylomata acuminata DOID_11169 [An anogenital venereal wart that results_in infection located_in mucosa of vagina, has_material_basis_in human papillomaviruses (types 6 and 11), which are transmitted_by direct sexual contact with the skin of an infected partner. The infection has_symptom vaginal warts.]