Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
erythrokeratodermia variabilis et progressiva 4	DOID_0080250
gum bleeding	SYMP_0000742	[Gum bleeding is a mouth symptom characterized by a copious discharge of blood from the blood vessels of the mucosal tissue that lies over the alveolar bone.]
mouth bleeding	SYMP_0000655
erythrokeratodermia variabilis et progressiva 5	DOID_0080251
enterobiasis	DOID_7457	[A parasitic helminthiasis infectious disease that involves infection of the anus by the pinworm Enterobius vermicularis. The major symptom is perianal itching. Infected people experience perianal pruritus and excoriations from scratching.]
anal canal carcinoma	DOID_6126	[An anal canal cancer that derives_from epithelial cells.]
spastic ataxia 8	DOID_0080252
spastic ataxia	DOID_0050952	[A hereditary ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy.]
genitourinary hemorrhage	SYMP_0000740
Meckel syndrome 13	DOID_0080253
amyotrophic neuralgia	DOID_10383
amyotrophic lateral sclerosis type 23	DOID_0080225
amyotrophic lateral sclerosis	DOID_332	[A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.]
obsolete papilledema associated with decreased ocular pressure	DOID_10384
autosomal dominant mental retardation 56	DOID_0080226	[A syndromic intellectual disability characterized by global developmental delay, intellectual disability and in most cases hypotonia, delayed walking, poor fine motor skills, and poor or absent speech that has_material_basis_in heterozygous mutation in the CLTC gene on chromosome 17q23.]
syndromic intellectual disability	DOID_0050888	[An intellectual disability that is characterized by the presence of associated medical and behavioral sign and symptoms.]
obsolete staphylococcal meningitis	DOID_10381
neurological alteration	SYMP_0000758
autosomal dominant mental retardation 55	DOID_0080227	[A syndromic intellectual disability characterized by onset of myoclonic seizures in the first years of life, global developmental delay, intellectual disability, speech delay and ataxic gait that has_material_basis_in heterozygous mutation in the NUS1 gene on chromosome 6q22.]
parotid pain	SYMP_0000759