All terms in DOID

Label Id Description
palpebral edema SYMP_0000344 [An adema that is characterized by an abnormal excess accumulation of serous fluid in connective tissue of the eyelids.]
aromatic carboxylic acid CHEBI_33859
slurred speech SYMP_0000342
rhabdoid tumor predisposition syndrome 1 DOID_0070618 [A rhabdoid tumor predisposition syndrome that has_material_basis_in heterozygous germline mutation in the SMARCB1 gene on chromosome 22q11.]
autoinflammation, antibody deficiency, and immune dysregulation syndrome DOID_0070615 [An autoimmune disease characterized by recurrent blistering skin lesions with a dense inflammatory infiltrate and variable involvement of other tissues, including joints, the eye, and the gastrointestinal tract that has_material_basis in heterozygous mutation in PLCG2 on chromosome 16q23.]
limb edema SYMP_0000340 [An adema that is characterized by an abnormal excess accumulation of serous fluid in connective tissue of the limbs.]
glycine encephalopathy 1 DOID_0070616 [A glycine encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the GLDC gene, a member of the mitochondrial glycine cleavage system that encodes the P protein, on chromosome 9p24.]
glycine encephalopathy DOID_9268 [An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues.]
premature labor SYMP_0000358 [A reproductive system symptom that is characterized by labor occurring before 37 full weeks of pregnancy.]
profound weakness SYMP_0000359
Brachyura NCBITaxon_6752
Pleocyemata NCBITaxon_6692
susceptibility to autosomal dominant parkinson disease 13 MIM_610297
Increased bone mineral density HP_0011001
Abnormality of bone mineral density HP_0004348
obsolete testicular mixed germ cell-sex cord-stromal neoplasm DOID_3580
Abnormality of metabolism/homeostasis HP_0001939
hypertrophic elongation of cervix DOID_2251
obsolete enterotoxemia DOID_3583
obsolete commensal Clostridium infectious disease DOID_3584