All terms in MONDO
| Label | Id | Description |
|---|---|---|
| mitochondrial complex II deficiency, nuclear type 1 | MONDO_0100294 | |
| Alzheimer disease, susceptibility to, mitochondrial | MONDO_0100295 | |
| Olmsted syndrome 1 | MONDO_0100296 | |
| short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1 | MONDO_0100297 | |
| PAX5-related B lymphopenia and autism spectrum disorder | MONDO_0100299 | |
| B cell deficiency | MONDO_0002211 | |
| autism spectrum disorder | MONDO_0005258 | |
| non-atopic asthma | MONDO_0800112 | |
| necrotizing vasculitis | MONDO_0800113 | |
| persistent tachypnoe of infancy, aberrant | MONDO_0800110 | |
| persistent tachypnoe of infancy | MONDO_0800109 | |
| persistent tachypnoe of infancy, usual | MONDO_0800111 | |
| cutaneous botryomycosis | MONDO_0800117 | |
| botryomycosis | MONDO_0400006 | |
| follicular bronchiolits | MONDO_0800114 | |
| idiopathic interstitial pneumonia | MONDO_0002429 | |
| visceral botryomycosis | MONDO_0800118 | |
| postinfectious bronchiolitis obliterans | MONDO_0800119 | |
| cystinosis | MONDO_0016239 | |
| DKC1-related disorder | MONDO_0100152 |