All terms in MONDO
| Label | Id | Description |
|---|---|---|
| renal hypodysplasia/aplasia 3 | MONDO_0024520 | |
| obsolete MONDO:0000575 | MONDO_0000575 | |
| obsolete CD45 deficiency | MONDO_0000574 | |
| recombinase activating gene 2 deficiency | MONDO_0000573 | |
| amyloidosis, primary localized cutaneous, 1 | MONDO_0024522 | |
| familial primary localized cutaneous amyloidosis | MONDO_0007101 | |
| aortic aneurysm, familial abdominal, 1 | MONDO_0024521 | |
| recombinase activating gene 1 deficiency | MONDO_0000572 | |
| dyschromatosis universalis hereditaria 1 | MONDO_0024524 | |
| obsolete coronin-1A deficiency | MONDO_0000579 | |
| aortic valve disease 1 | MONDO_0024523 | |
| familial bicuspid aortic valve | MONDO_0007194 | |
| obsolete CD3gamma deficiency | MONDO_0000578 | |
| Zimmermann-Laband syndrome 1 | MONDO_0024526 | |
| Fanconi renotubular syndrome 1 | MONDO_0024525 | |
| obsolete CD3delta deficiency | MONDO_0000576 | |
| Kostmann syndrome | MONDO_0012548 | |
| autosomal recessive ataxia, Beauce type | MONDO_0012549 | |
| obsolete CD3zeta deficiency | MONDO_0000571 | |
| obsolete severe combined immunodeficiency due to artemis deficiency | MONDO_0000570 |