All terms in MONDO
| Label | Id | Description |
|---|---|---|
| sebaceous gland anomaly | MONDO_0019286 | |
| acute tricyclic antidepressant poisoning | MONDO_0018547 | |
| poisoning | MONDO_0029000 | |
| serotonin syndrome | MONDO_0018546 | |
| nervous system disorder | MONDO_0005071 | |
| obsolete late-onset scapuloperoneal muscular dystrophy with hyaline bodies | MONDO_0018549 | |
| acute poisoning by drugs with membrane-stabilizing effect | MONDO_0018548 | |
| autosomal dominant hypocalcemia | MONDO_0018543 | |
| familial hypoparathyroidism | MONDO_0016390 | |
| calcium metabolic disease | MONDO_0005557 | |
| autosomal dominant disease | MONDO_0000426 | |
| severe congenital neutropenia | MONDO_0018542 | |
| constitutional neutropenia | MONDO_0015134 | |
| obsolete primary immunodeficiency with predisposition to severe viral infection | MONDO_0018545 | |
| familial severe combined immunodeficiency | MONDO_0031520 | |
| severe combined immunodeficiency | MONDO_0015974 | |
| adrenoleukodystrophy | MONDO_0018544 | |
| X-linked disease | MONDO_0000425 | |
| disorder of peroxisomal transporter | MONDO_0100372 | |
| genetic dementia | MONDO_0015547 |