All terms in DOID

Label Id Description
obsolete vesicoureteral reflux with reflux nephropathy DOID_13696
short-rib thoracic dysplasia 7 with or without polydactyly DOID_0110090 [An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WDR35 gene on chromosome 2p21.1.]
developmental coordination disorder DOID_9923 [A specific developmental disorder that involves disordered motor skills where coordinated muscle movement is impaired.]
short-rib thoracic dysplasia 10 with or without polydactyly DOID_0110091 [An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the IFT172 gene on chromosome 2p23.]
obsolete hyperostosis frontalis interna DOID_9925
hair of head UBERON_0016446
bronchopneumonia DOID_12375 [A pneumonia involving inflammation of lungs that begins in the terminal bronchioles, which become clogged with thick mucus that forms consolidated patches in adjacent lobules. It is caused by bacteria and viruses.]
arrhythmogenic right ventricular dysplasia 8 DOID_0110076 [An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the gene encoding desmoplakin (DSP) on chromosome 6p24.]
gastroschisis DOID_11044
arrhythmogenic right ventricular dysplasia 9 DOID_0110077 [An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutations in the PKP2 gene on chromosome 12p11.]
obsolete moderate degree recurrent episode manic disease DOID_8609
arrhythmogenic right ventricular dysplasia 5 DOID_0110074 [An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the TMEM43 gene on chromosome 3p25.]
Felty's syndrome DOID_11042 [An autoimmune disease that results_in rheumatoid arthritis, splenomegaly and neutropenia.]
arrhythmogenic right ventricular dysplasia 6 DOID_0110075 [An arrhythmogenic right ventricular dysplasia associated with variation in the region 10p14-p12.]
arrhythmogenic right ventricular dysplasia 3 DOID_0110072 [An arrhythmogenic right ventricular dysplasia associated with variation in the region 14q12-q22.]
arrhythmogenic right ventricular dysplasia 4 DOID_0110073 [An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3.]
arrhythmogenic right ventricular dysplasia 1 DOID_0110070 [An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the TGFB3 gene on chromosome 14q24.]
obsolete arrhythmogenic right ventricular dysplasia 2 DOID_0110071 [An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the cardiac ryanodine receptor-2 gene (RYR2) on chromosome 1q43.]
Arvicolinae NCBITaxon_39087
meconium aspiration syndrome DOID_11049 [A lung disease that is characterized by a newborn breathing in a mixture of meconium and amniotic fluid into the lungs around the time of delivery.]