All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Oguchi disease | MONDO_0019152 | |
| entropion | MONDO_0001519 | |
| auriculoosteodysplasia | MONDO_0007177 | |
| aurocephalosyndactyly | MONDO_0007178 | |
| PR interval, variation in | MONDO_0007175 | |
| helicoid peripapillary chorioretinal degeneration | MONDO_0007176 | |
| obsolete rare eyelid malformation | MONDO_0020152 | |
| alopecia, androgenetic, 1 | MONDO_0007184 | |
| Banki syndrome | MONDO_0007185 | |
| azotemia, familial | MONDO_0007183 | |
| Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities | MONDO_0007180 | |
| axial osteomalacia | MONDO_0007181 | |
| obsolete early-onset ataxia with dementia | MONDO_0020139 | |
| obsolete ataxia with dementia | MONDO_0020138 | |
| obsolete strongyloidiasis | MONDO_0019166 | |
| pyomyositis | MONDO_0019168 | |
| immunoglobulin a vasculitis | MONDO_0019167 | |
| obsolete late-onset ataxia with dementia | MONDO_0020140 | |
| 6q terminal deletion syndrome | MONDO_0019164 | |
| obsolete pseudoxanthoma elasticum | MONDO_0019163 |