| Label | Id | |
|---|---|---|
| night blindness, congenital stationary, type1i | 32811 | |
| autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1 | 8119 | |
| autosomal recessive cerebellar ataxia-saccadic intrusion syndrome | 11811 | |
| high altitude cerebral edema | 21811 | |
| cancer, sigmoid colon | D012811 | |
| neoplasm, sigmoid colon | D012811 | |
| neoplasms, sigmoid colon | D012811 | |
| Feingold syndrome caused by mutation in MYCN | 8115 | |
| trisomy 3p chromosome 3 | C536811 | |
| trisomy 6p chromosome 6 | C537811 | |
| simple chronic conjunctivitis | 4811 | |
| situs inversus, complex cardiac defects, and splenic defects, X-linked | C538116 | |
| anomalous left coronary artery from the pulmonary artery | 811 | |
| vitamin e deficiency | D014811 | |
| dystonia musculorum deformans | 44811 |