All terms in MONDO
| Label | Id | Description |
|---|---|---|
| oculocutaneous albinism type 3 | MONDO_0008747 | |
| oculocutaneous albinism type 2 | MONDO_0008746 | |
| obsolete fetal alcohol spectrum disorders | MONDO_0021720 | |
| oculocutaneous albinism type 1A | MONDO_0008745 | |
| autosomal recessive ocular albinism | MONDO_0040653 | |
| oculocutaneous albinism type 1 | MONDO_0018135 | |
| alar cartilages hypoplasia-coloboma-telecanthus syndrome | MONDO_0008744 | |
| Stimmler syndrome | MONDO_0008743 | |
| autosomal dominant severe congenital neutropenia | MONDO_0008742 | |
| PAGOD syndrome | MONDO_0008741 | |
| syndromic uterovaginal malformation | MONDO_0015846 | |
| agnathia-otocephaly complex | MONDO_0008740 | |
| alcohol amnestic disorder | MONDO_0021702 | |
| alcohol-related disorders | MONDO_0021698 | |
| amnestic disorder | MONDO_0001152 | |
| oxoglutaricaciduria | MONDO_0008759 | |
| metabolic epilepsy | MONDO_0100033 | |
| tricarboxylic acid cycle disorder | MONDO_0016790 | |
| mitochondrial DNA depletion syndrome 4a | MONDO_0008758 | |
| alopecia universalis congenita | MONDO_0008757 |