All terms in MONDO
| Label | Id | Description |
|---|---|---|
| chromosome 13q trisomy | MONDO_0022177 | |
| chromosome 13q-mosaicism | MONDO_0022178 | |
| chromhidrosis | MONDO_0022171 | |
| chromosome 11q trisomy | MONDO_0022173 | |
| chromosome 12p deletion | MONDO_0022174 | |
| ethanolaminosis | MONDO_0009199 | |
| early-onset calcifying leukoencephalopathy-skeletal dysplasia | MONDO_0034143 | |
| pancreatic agenesis-holoprosencephaly syndrome | MONDO_0034142 | |
| whistling face syndrome, recessive form | MONDO_0010197 | |
| white forelock with malformations | MONDO_0010199 | |
| pontocerebellar hypoplasia type 2A | MONDO_0010190 | |
| Waardenburg syndrome type 4A | MONDO_0010192 | |
| Waardenburg-Shah syndrome | MONDO_0019518 | |
| von Willebrand disease 3 | MONDO_0010191 | |
| neonatal epileptic encephalopathy due to glutaminase deficiency | MONDO_0034147 | |
| Weill-Marchesani syndrome 1 | MONDO_0010194 | |
| spastic ataxia-dysarthria due to glutaminase deficiency | MONDO_0034146 | |
| autosomal recessive spastic ataxia | MONDO_0017847 | |
| Weaver syndrome | MONDO_0010193 | |
| Werner syndrome | MONDO_0010196 |