All terms in MONDO
| Label | Id | Description |
|---|---|---|
| trisomy X | MONDO_0018066 | |
| chromosome X disorder | MONDO_0700027 | |
| arthrogryposis, distal, IIa 11 | MONDO_0031045 | |
| distal arthrogryposis | MONDO_0019942 | |
| isolated trigonocephaly | MONDO_0018065 | |
| isolated craniosynostosis | MONDO_0015337 | |
| trigonocephaly | MONDO_0000156 | |
| trisomy 13 | MONDO_0018068 | |
| chromosome 13 disorder | MONDO_0700020 | |
| syndromic anorectal malformation | MONDO_0015246 | |
| congenital vitreoretinal dysplasia | MONDO_0020247 | |
| lymphatic malformation 12 | MONDO_0031043 | |
| triploidy | MONDO_0018067 | |
| polyploidy | MONDO_0019934 | |
| autosomal dominant trichoodontoonychodysplasia-syndactyly | MONDO_0018062 | |
| trichodermodysplasia-dental alterations syndrome | MONDO_0018061 | |
| trigonocephaly-broad thumbs syndrome | MONDO_0018064 | |
| nodular non-suppurative panniculitis | MONDO_0018063 | |
| congenital fibrinogen deficiency | MONDO_0018060 | |
| coagulation protein disease | MONDO_0002242 |