All terms in MONDO
| Label | Id | Description |
|---|---|---|
| autoimmune inner ear disease | MONDO_0022518 | |
| autoimmune myocarditis | MONDO_0022519 | |
| autoimmune cardiomyopathy | MONDO_0030701 | |
| X-linked progressive cerebellar ataxia | MONDO_0010547 | |
| Hennekam-Beemer syndrome | MONDO_0009569 | |
| central incisors, absence of | MONDO_0010546 | |
| mast syndrome | MONDO_0009568 | |
| Charcot-Marie-Tooth disease X-linked dominant 1 | MONDO_0010549 | |
| Marinesco-Sjogren syndrome | MONDO_0009567 | |
| spinocerebellar ataxia, X-linked 2 | MONDO_0010548 | |
| marfanoid habitus-autosomal recessive intellectual disability syndrome | MONDO_0009566 | |
| microcephaly-glomerulonephritis-marfanoid habitus syndrome | MONDO_0009565 | |
| Marden-Walker syndrome | MONDO_0009564 | |
| beta-mannosidosis | MONDO_0009562 | |
| autosomal recessive familial Mediterranean fever | MONDO_0009572 | |
| Coffin-Lowry syndrome | MONDO_0010561 | |
| Meckel syndrome, type 1 | MONDO_0009571 | |
| cleft palate with or without ankyloglossia, X-linked | MONDO_0010560 | |
| McDonough syndrome | MONDO_0009570 | |
| blue cone monochromacy | MONDO_0010563 |