Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete primary hypotonic uterine dysfunction	DOID_8490
autosomal recessive nonsyndromic deafness 111	DOID_0111640	[An autosomal recessive nonsyndromic deafness characterized by early-onset, moderate to severe sensorineural hearing loss with no vestibular involvement that has_material_basis_in homozygous or compound heterozygous mutation in MPZL2 on chromosome 11q23.33.]
rectum leiomyoma	DOID_7160
rectum adenoma	DOID_0050915	[An rectal neoplasm that has_material_basis_in epithelial tissue with glandular origin.]
obsolete Prolonged first stage of labor	DOID_8491
autosomal recessive nonsyndromic deafness 94	DOID_0111641	[An autosomal recessive nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in NARS2 on chromosome 11q14.1.]
hypertrophic cardiomyopathy 4	DOID_0110310	[A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11.]
mucormycosis	DOID_8485	[An opportunistic mycosis that results_in fungal infection located_in sinuses, located_in brain, or located_in lungs of immunocompromised people, has_material_basis_in Mucorales molds.]
obsolete anaplastic oligodendroglioma	DOID_7154
obsolete adult undifferentiated oligodendroglioma	DOID_7155
prostate stromal sarcoma	DOID_7152	[A stromal sarcoma and sarcoma of prostate and tumor of specialized prostatic stroma that is located_in the prostate.]
maple bark strippers' lung	DOID_8484	[An opportunistic mycosis that is located_in lungs caused by inhalation of fungal spores while stripping the bark from maple logs, has_material_basis_in Cryptostroma corticale.]
obsolete disorder of amniotic fluid and membranes	DOID_8489
obsolete recurrent metastatic squamous cell cancer to the neck with occult primary	DOID_7158
interstitial cystitis	DOID_13949
hypertrophic cardiomyopathy 13	DOID_0110319	[A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.]
bladder neck obstruction	DOID_13948
obsolete secondary retinal cyst	DOID_8487
obsolete anaplastic childhood oligodendroglioma	DOID_7156
ectopia lentis with ectopia of pupil	DOID_0111648	[An eye disease characterized by displacement of the lenses and the pupils in association with other ocular anomalies that has_material_basis_in homozygous or compound heterozygous mutation mutation in ADAMTSL4 on chromosome 1q21.2.]