All terms in MONDO
| Label | Id | Description |
|---|---|---|
| obsolete gastric sneezing | MONDO_0007645 | |
| Gamstorp-Wohlfart syndrome | MONDO_0007646 | |
| gamma-A-globulin, defect in assembly of | MONDO_0007643 | |
| IgAD1 | MONDO_0007644 | |
| obsolete Futcher line | MONDO_0007641 | |
| isolated agenesis of gallbladder | MONDO_0007642 | |
| Sorsby fundus dystrophy | MONDO_0007640 | |
| congenital megacalycosis | MONDO_0019639 | |
| microcephaly, growth restriction, and increased sister chromatid exchange 2 | MONDO_0020628 | |
| epileptic encephalopathy, infantile or early childhood | MONDO_0020627 | |
| obsolete yt blood group antigen | MONDO_0020626 | |
| renal agenesis, unilateral | MONDO_0019636 | |
| obsolete blood group--wright antigen | MONDO_0020625 | |
| idiopathic achalasia | MONDO_0019635 | |
| obsolete blood group--waldner type | MONDO_0020624 | |
| renal dysplasia | MONDO_0019638 | |
| obsolete blood group--ul system | MONDO_0020623 | |
| renal hypoplasia | MONDO_0019637 | |
| obsolete blood group--stoltzfus system | MONDO_0020622 | |
| mitochondrial complex 1 deficiency, nuclear type 5 | MONDO_0032610 |