All terms in MONDO
| Label | Id | Description |
|---|---|---|
| ataxia-telangiectasia-like disorder | MONDO_0011457 | |
| coenzyme Q10 deficiency | MONDO_0018151 | |
| ataxia-telangiectasia with generalized skin pigmentation and early death | MONDO_0008841 | |
| ataxia telangiectasia | MONDO_0008840 | |
| inherited nervous system cancer-predisposing syndrome | MONDO_0016756 | |
| combined immunodeficiency | MONDO_0015131 | |
| acute cholinergic dysautonomia | MONDO_0021808 | |
| primary dysautonomia | MONDO_0021809 | |
| dysautonomia | MONDO_0044872 | |
| silicotuberculosis | MONDO_0021804 | |
| acromesomelic dysplasia, Campailla Martinelli type | MONDO_0021805 | |
| acromesomelic dysplasia | MONDO_0019696 | |
| berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification | MONDO_0008859 | |
| Behr syndrome | MONDO_0008858 | |
| OPA1-related optic atrophy with or without extraocular features | MONDO_0800181 | |
| Beemer-Ertbruggen syndrome | MONDO_0008857 | |
| immunodeficiency 27A | MONDO_0008856 | |
| inherited susceptibility to mycobacterial diseases | MONDO_0019146 | |
| MHC class II deficiency | MONDO_0008855 | |
| Bardet-Biedl syndrome 1 | MONDO_0008854 |