All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Bonnevie-Ullrich syndrome | MONDO_0100492 | |
| autosomal recessive titinopathy | MONDO_0100493 | |
| TTN-related myopathy | MONDO_0100175 | |
| autosomal dominant titinopathy | MONDO_0100494 | |
| autosomal recessive distal titinopathy | MONDO_0100495 | |
| Emery-Dreifuss-like muscular dystrophy | MONDO_0100496 | |
| titinopathy with congenital contractures | MONDO_0100497 | |
| UROD-related inherited porphyria | MONDO_0100498 | |
| inherited porphyria | MONDO_0019142 | |
| reactive airway disease | MONDO_0100470 | |
| vitamin D deficiency | MONDO_0100471 | |
| vitamin deficiency disorder | MONDO_0024298 | |
| disorder of peptide and amine metabolism | MONDO_0100473 | |
| mild ichthyosis vulgaris | MONDO_0100474 | |
| autosomal dominant ichthyosis vulgaris | MONDO_0007810 | |
| severe ichthyosis vulgaris | MONDO_0100475 | |
| lipodystrophy, partial, acquired, susceptibility to | MONDO_0100476 | |
| acquired partial lipodystrophy | MONDO_0012104 | |
| disorder of methylamine metabolism | MONDO_0100477 | |
| brain malformations with or without urinary tract defects | MONDO_0100478 |