All terms in MONDO
| Label | Id | Description |
|---|---|---|
| arterial calcification, generalized, of infancy, 1 | MONDO_0008817 | |
| arterial calcification of infancy | MONDO_0018870 | |
| Chiari malformation type II | MONDO_0008816 | |
| Chiari malformation | MONDO_0000115 | |
| spina bifida cystica | MONDO_0017069 | |
| argininosuccinic aciduria | MONDO_0008815 | |
| amino acid metabolism disease | MONDO_0037871 | |
| hyperargininemia | MONDO_0008814 | |
| arachnoid cyst | MONDO_0008813 | |
| central nervous system cystic malformation | MONDO_0017104 | |
| AREDYLD syndrome | MONDO_0008812 | |
| XK aprosencephaly | MONDO_0008811 | |
| familial apolipoprotein C-II deficiency | MONDO_0008810 | |
| familial chylomicronemia syndrome | MONDO_0018637 | |
| arteriosclerosis, severe juvenile | MONDO_0008819 | |
| chylous ascites | MONDO_0008829 | |
| camptodactyly-arthropathy-coxa vara-pericarditis syndrome | MONDO_0008828 | |
| rheumatic disorder | MONDO_0005554 | |
| progressive pseudorheumatoid arthropathy of childhood | MONDO_0008827 | |
| genetic inflammatory or rheumatoid-like osteoarthropathy | MONDO_0800092 |