All terms in DOID

Label Id Description
hereditary lymphedema I DOID_0070212 [A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood.]
Viridiplantae NCBITaxon_33090
Eukaryota NCBITaxon_2759
right lower quadrant abdominal tenderness SYMP_0000500
familial hyperinsulinemic hypoglycemia 1 DOID_0070219 [A hyperinsulinemic hypoglycemia characterized by autosomal recessive inheritance of hyperinsulinemic hypoglycemia that is resistant to diazoxide treatment that has_material_basis_in mutation in the ABCC8 gene on chromosome 11p15.]
generalized abdominal pain SYMP_0000518 [An abdominal pain that is characterized by being diffuse or widespread and affecting or involving all of the abdomen.]
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.]