All terms in DOID

Label Id Description
Pulicidae NCBITaxon_7511
Fasciolidae NCBITaxon_27843
central nervous system neuron CL_2000029
Echinostoma NCBITaxon_27847
acrocallosal syndrome DOID_9250 [A syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation.]
Phlebotomus <genus> NCBITaxon_13203
Phlebotominae NCBITaxon_7198
Alagille syndrome DOID_9245 [A liver disease that is characterized by an accumulation of bile in the liver resulting from a reducted number of liver small bile ducts.]
Beemer-Langer syndrome DOID_9249 [A syndrome that results_in multiple congenital anomalies, including hydrops fetalis, facial and visceral abnormalities, short ribs, and short limbs without polydactyly.]
Pallister-Hall syndrome DOID_9248 [A syndrome that is characterized by hypothalamic hamartoma, pituitary dysfunction, central polydactyly, and visceral malformations and has_material_basis_in autosomal dominant heterozygous mutation in the GLI3 gene on chromosome 7p14.]
Abnormal circulating dicarboxylic acid concentration HP_0010995
Abnormal circulating carboxylic acid concentration HP_0004354
Abnormal cerebral morphology HP_0002060
terpene lactone CHEBI_37668
sesquiterpenoid CHEBI_26658
lactone CHEBI_25000
Dermacentor marginatus NCBITaxon_49202
Nidovirales NCBITaxon_76804
organic ion CHEBI_25699
organic cation CHEBI_25697