All terms in DOID

Label Id Description
oxoacid derivative CHEBI_33241
sulfur molecular entity CHEBI_26835
abnormal feces SYMP_0000519
lump in chest SYMP_0000516
hemoptysis SYMP_0000517 [A respiratory system and chest symptom that is characterized by an expectoration of blood from some part of the respiratory tract.]
hiccough SYMP_0000515 [A respiratory system and chest symptom that is characterized by a spasmodic inhalation with closure of the glottis accompanied by a peculiar sound.]
male stress incontinence SYMP_0000512 [A stress incontinence that is characterized by a compromised external urinary sphincter muscle resulting from surgical or radiotherapeutic manipulation.]
stress incontinence SYMP_0000853 [A urinary incontinence that is characterized by an involuntary leakage of urine from the bladder accompanying physical activity (as in laughing, coughing, sneezing, or physical exercise) which places increased pressure on the abdomen.]
stridor SYMP_0000513 [An abnormal chest sound that is characterized by a harsh vibrating sound heard during respiration in cases of obstruction of the air passages.]
Parkinson's disease DOID_14330 [A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.]
Parkinson's disease 4 DOID_0060895 [A late onset Parkinson disease that has_material_basis_in heterozygous triplication of the alpha-synuclein gene on chromosome 4q22.]
late onset Parkinson's disease DOID_0060892 [A Parkinson's disease characterized by onset of motor symptoms typically after 60 years of age.]
Parkinson's disease 23 DOID_0060896 [An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.]
Parkinson's disease 17 DOID_0060897 [A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13.]
Parkinson's disease 20 DOID_0060898 [An early-onset Parkinson disease that has_material_basis_in homozygous mutation in the SYNJ1 gene on chromosome 21q22.]
ectopic Cushing syndrome DOID_0060890 [A primary hyperaldosteronism that is characterized by a tumor outside the pituitary gland produces a hormone called adrenocorticotropic hormone.]
primary hyperaldosteronism DOID_446 [An adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands.]
Parkinson's disease 19A DOID_0060891 [An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.]
juvenile-onset Parkinson's disease DOID_0060893 [An early-onset Parkinson's disease that is characterized by onset of motor symptoms prior to 21 years of age.]
pallor SYMP_0000510 [A skin and integumentary tissue symptom that is characterized by a deficiency of color especially of the face.]