All terms in MONDO
| Label | Id | Description |
|---|---|---|
| keratinopathic ichthyosis | MONDO_0017266 | |
| ichthyosis-cheek-eyebrow syndrome | MONDO_0007811 | |
| tracheomalacia | MONDO_0019804 | |
| mesocardia | MONDO_0019807 | |
| primary adrenal insufficiency | MONDO_0015128 | |
| chronic hepatic porphyria | MONDO_0019800 | |
| secondary short bowel syndrome | MONDO_0019802 | |
| hyper-IgE recurrent infection syndrome 1 | MONDO_0007818 | |
| solitary median maxillary central incisor syndrome | MONDO_0007819 | |
| holoprosencephaly 3 | MONDO_0007733 | |
| inclusion body myositis | MONDO_0007827 | |
| indifference to pain, congenital, autosomal dominant | MONDO_0007828 | |
| incisors, rotation of upper central | MONDO_0007825 | |
| incisors, shovel-shaped | MONDO_0007826 | |
| obsolete insulin receptors, familial increase 1N | MONDO_0007823 | |
| incisors, lower central, absence of | MONDO_0007824 | |
| obsolete immunoglobulin switch sequences | MONDO_0007821 | |
| obsolete incisors, long upper central | MONDO_0007822 | |
| fused mandibular incisors | MONDO_0007820 | |
| anomaly of the tricuspid subvalvular apparatus | MONDO_0019816 |